A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700963



Internal ID15437615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8395652..8412104hg38UCSC Ensembl
Innerchr1:8455712..8472164hg19UCSC Ensembl
Innerchr1:8378299..8394751hg18UCSC Ensembl
Innerchr1:8389978..8406430hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3816453
hg1916453
hg1816453
hg1716453
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524946
Supporting Variants
Samples
Known GenesRERE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700963
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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