A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636778



Internal ID7023572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67287529..67290752hg38UCSC Ensembl
Innerchr15:67287529..67290752hg38UCSC Ensembl
Outerchr15:67287143..67291056hg38UCSC Ensembl
chr15:67579867..67583090hg19UCSC Ensembl
Innerchr15:67579867..67583090hg19UCSC Ensembl
Outerchr15:67579481..67583394hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383224
hg193224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15275359, essv15275360, essv15275358, essv15275357, essv15275361, essv15275350, essv15275353, essv15275348, essv15275356, essv15275355, essv15275349, essv15275352, essv15275354, essv15275351
SamplesHG01412, HG01325, HG01351, HG02252, HG01950, HG01142, HG02102, HG01094, HG01921, NA19752, HG01494, HG01479, NA19661, NA18997
Known GenesIQCH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636778
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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