A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666570



Internal ID15403222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68532128..68539492hg38UCSC Ensembl
Innerchr6:69242020..69249384hg19UCSC Ensembl
Innerchr6:69298741..69306105hg18UCSC Ensembl
Innerchr6:69298741..69306105hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg387365
hg197365
hg187365
hg177365
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515885
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666570
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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