A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704699



Internal ID15441351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24359755..24366837hg38UCSC Ensembl
Innerchr15:24604902..24611984hg19UCSC Ensembl
Innerchr15:22155995..22163077hg18UCSC Ensembl
Innerchr15:22155995..22163077hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387083
hg197083
hg187083
hg177083
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704699
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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