A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672970



Internal ID15062936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10469593..10518117hg38UCSC Ensembl
Innerchr6:10469826..10518350hg19UCSC Ensembl
Innerchr6:10577812..10626336hg18UCSC Ensembl
Innerchr6:10577812..10626336hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3848525
hg1948525
hg1848525
hg1748525
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520598
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672970
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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