A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637114



Internal ID7023908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85406372..85411010hg38UCSC Ensembl
Innerchr15:85406373..85411010hg38UCSC Ensembl
Outerchr15:85406372..85411011hg38UCSC Ensembl
chr15:85949603..85954241hg19UCSC Ensembl
Innerchr15:85949604..85954241hg19UCSC Ensembl
Outerchr15:85949603..85954242hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384639
hg194639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15314307, essv15314315, essv15314334, essv15314292, essv15314327, essv15314341, essv15314287, essv15314343, essv15314293, essv15314322, essv15314291, essv15314331, essv15314354, essv15314328, essv15314319, essv15314333, essv15314351, essv15314353, essv15314296, essv15314298, essv15314316, essv15314289, essv15314313, essv15314300, essv15314297, essv15314356, essv15314342, essv15314355, essv15314306, essv15314340, essv15314317, essv15314294, essv15314308, essv15314295, essv15314324, essv15314349, essv15314304, essv15314303, essv15314347, essv15314339, essv15314318, essv15314352, essv15314321, essv15314335, essv15314312, essv15314332, essv15314286, essv15314288, essv15314345, essv15314325, essv15314348, essv15314310, essv15314290, essv15314330, essv15314299, essv15314344, essv15314337, essv15314305, essv15314302, essv15314320, essv15314311, essv15314329, essv15314301, essv15314350, essv15314326, essv15314323, essv15314336, essv15314309, essv15314346, essv15314338, essv15314314
SamplesHG01985, HG02574, NA20339, HG03559, NA19222, HG02496, HG03517, HG03247, HG03057, HG02337, HG03298, NA18878, HG03515, NA18519, HG03385, HG03452, NA20320, NA19307, HG01968, HG03246, HG02816, HG02981, NA19917, HG03380, NA19189, HG03114, HG02716, NA19437, NA19152, NA19984, NA19184, NA19043, HG02108, HG02953, HG02757, NA19114, HG03136, HG03388, NA19113, HG03024, HG02979, NA19225, HG02568, HG01956, HG03240, NA19256, HG02799, NA19019, NA19454, HG01915, HG03458, HG02837, NA19144, NA19835, HG02941, NA19467, HG03473, HG02317, HG03557, HG02771, NA18501, HG03112, HG02095, HG01085, HG02676, NA19121, HG03162, HG02855, HG02851, HG02284, HG03129
Known GenesAKAP13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637114
Frequency
Sample Size2504
Observed Gain0
Observed Loss71
Observed Complex0
Frequencyn/a


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