A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697353



Internal ID15434005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123591621..123592849hg38UCSC Ensembl
Innerchr6:123912766..123913994hg19UCSC Ensembl
Innerchr6:123954465..123955693hg18UCSC Ensembl
Innerchr6:123954465..123955693hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381229
hg191229
hg181229
hg171229
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520332
Supporting Variants
Samples
Known GenesTRDN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697353
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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