A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696770



Internal ID15086736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29577938..29591518hg38UCSC Ensembl
Innerchr6:29545715..29559295hg19UCSC Ensembl
Innerchr6:29653694..29667274hg18UCSC Ensembl
Innerchr6:29653694..29667274hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3813581
hg1913581
hg1813581
hg1713581
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519288
Supporting Variants
Samples
Known GenesOR2H2, SNORD32B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696770
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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