A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639923



Internal ID7026701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9778120..9786051hg38UCSC Ensembl
Innerchr17:9778270..9785901hg38UCSC Ensembl
Outerchr17:9777970..9786201hg38UCSC Ensembl
chr17:9681437..9689368hg19UCSC Ensembl
Innerchr17:9681587..9689218hg19UCSC Ensembl
Outerchr17:9681287..9689518hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387932
hg197932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15610365, essv15610371, essv15610372, essv15610370, essv15610363, essv15610366, essv15610367, essv15610362, essv15610364, essv15610369, essv15610368
SamplesHG00766, HG00452, HG02087, HG02166, HG02084, HG01029, HG02408, HG01028, HG01817, HG01872, HG02406
Known GenesDHRS7C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639923
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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