A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689559



Internal ID15426211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97770312..97793614hg38UCSC Ensembl
Innerchr7:97399624..97422926hg19UCSC Ensembl
Innerchr7:97237560..97260862hg18UCSC Ensembl
Innerchr7:97044275..97067577hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3823303
hg1923303
hg1823303
hg1723303
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516307
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689559
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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