A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636829



Internal ID7023623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69961710..69965912hg38UCSC Ensembl
Innerchr15:69961710..69965912hg38UCSC Ensembl
Outerchr15:69961465..69966157hg38UCSC Ensembl
chr15:70254049..70258251hg19UCSC Ensembl
Innerchr15:70254049..70258251hg19UCSC Ensembl
Outerchr15:70253804..70258496hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384203
hg194203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15280232, essv15280254, essv15280252, essv15280246, essv15280257, essv15280249, essv15280229, essv15280256, essv15280245, essv15280236, essv15280231, essv15280234, essv15280243, essv15280241, essv15280235, essv15280228, essv15280251, essv15280238, essv15280230, essv15280244, essv15280239, essv15280237, essv15280250, essv15280242, essv15280226, essv15280233, essv15280253, essv15280247, essv15280248, essv15280255, essv15280227, essv15280240
SamplesHG01456, HG02589, NA20356, HG03082, HG03464, HG03091, HG02620, NA19916, HG02562, HG02561, NA20278, NA18868, HG02642, HG02471, NA19456, HG02570, NA19707, HG03061, HG03081, HG02470, HG03136, HG02585, HG03567, NA19147, HG02308, HG03469, HG02839, HG02051, HG03445, HG02763, HG02861, NA19312
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636829
Frequency
Sample Size2504
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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