A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047590



Internal ID15554090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:403799..833579hg38UCSC Ensembl
Innerchr6:403799..833579hg19UCSC Ensembl
Innerchr6:348799..778579hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38429781
hg19429781
hg18429781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600781
Supporting Variants
Samples
Known GenesEXOC2, HUS1B, IRF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047590
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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