A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655391



Internal ID18606986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163421326..163544184hg38UCSC Ensembl
Innerchr6:163842358..163965216hg19UCSC Ensembl
Innerchr6:163762348..163885206hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38122859
hg19122859
hg18122859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019551
Supporting Variants
Samples
Known GenesQKI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655391
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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