A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661082



Internal ID15397734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149088724..149088996hg38UCSC Ensembl
Innerchr6:149409860..149410132hg19UCSC Ensembl
Innerchr6:149451553..149451825hg18UCSC Ensembl
Innerchr6:149451553..149451825hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38273
hg19273
hg18273
hg17273
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520134
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661082
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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