A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656266



Internal ID15392918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40036301..40061443hg38UCSC Ensembl
Innerchr6:40004040..40029182hg19UCSC Ensembl
Innerchr6:40112018..40137160hg18UCSC Ensembl
Innerchr6:40112018..40137160hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3825143
hg1925143
hg1825143
hg1725143
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515601
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656266
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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