A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751324



Internal ID18725570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65581289..65581430hg38UCSC Ensembl
Outerchr15:65581273..65581449hg38UCSC Ensembl
Innerchr15:65873627..65873768hg19UCSC Ensembl
Outerchr15:65873611..65873787hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552577
Supporting Variants
Samples
Known GenesVWA9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751324
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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