A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700844



Internal ID15437496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112569317..112574931hg38UCSC Ensembl
Innerchr6:112890519..112896133hg19UCSC Ensembl
Innerchr6:112997212..113002826hg18UCSC Ensembl
Innerchr6:112997212..113002826hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385615
hg195615
hg185615
hg175615
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524842
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700844
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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