A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668654



Internal ID15058620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:162365634..162390640hg38UCSC Ensembl
Innerchr1:162335424..162360430hg19UCSC Ensembl
Innerchr1:160602048..160627054hg18UCSC Ensembl
Innerchr1:159067082..159092088hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3825007
hg1925007
hg1825007
hg1725007
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516482
Supporting Variants
Samples
Known GenesC1orf111, C1orf226, NOS1AP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668654
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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