A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701826



Internal ID15091792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27655732..27689868hg38UCSC Ensembl
Innerchr6:27623511..27657647hg19UCSC Ensembl
Innerchr6:27731490..27765626hg18UCSC Ensembl
Innerchr6:27731490..27765626hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3834137
hg1934137
hg1834137
hg1734137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525669
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701826
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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