A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697989



Internal ID15434641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69506370..69551415hg38UCSC Ensembl
Innerchr6:70216262..70261307hg19UCSC Ensembl
Innerchr6:70272983..70318028hg18UCSC Ensembl
Innerchr6:70272983..70318028hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3845046
hg1945046
hg1845046
hg1745046
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521380
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697989
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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