A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892709



Internal ID19183529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64335104..64418975hg38UCSC Ensembl
Outerchr15:64335104..64418975hg38UCSC Ensembl
Innerchr15:64627303..64711174hg19UCSC Ensembl
Outerchr15:64627303..64711174hg19UCSC Ensembl
Innerchr15:62414356..62498227hg18UCSC Ensembl
Outerchr15:62414356..62498227hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3883872
hg1983872
hg1883872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783926, essv25783937
Samples
Known GenesCSNK1G1, KIAA0101, TRIP4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892709
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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