A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702072



Internal ID15438724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:205292046..205294176hg38UCSC Ensembl
Innerchr1:205261174..205263304hg19UCSC Ensembl
Innerchr1:203527797..203529927hg18UCSC Ensembl
Innerchr1:201992831..201994961hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382131
hg192131
hg182131
hg172131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525872
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702072
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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