A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689533



Internal ID15426185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166789305..166789500hg38UCSC Ensembl
Innerchr1:166758542..166758737hg19UCSC Ensembl
Innerchr1:165025166..165025361hg18UCSC Ensembl
Innerchr1:163490200..163490395hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38196
hg19196
hg18196
hg17196
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519275
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689533
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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