A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075613



Internal ID15582113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163414042..163415602hg38UCSC Ensembl
Innerchr6:163835074..163836634hg19UCSC Ensembl
Innerchr6:163755064..163756624hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381561
hg191561
hg181561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605206
Supporting Variants
Samples
Known GenesQKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075613
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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