A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654585



Internal ID15044551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:162339489..162342193hg38UCSC Ensembl
Innerchr1:162309279..162311983hg19UCSC Ensembl
Innerchr1:160575903..160578607hg18UCSC Ensembl
Innerchr1:159040937..159043641hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382705
hg192705
hg182705
hg172705
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516482
Supporting Variants
Samples
Known GenesNOS1AP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654585
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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