A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603776



Internal ID16391185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76378484..76390536hg38UCSC Ensembl
Innerchr6:77088201..77100253hg19UCSC Ensembl
Innerchr6:77144921..77156973hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3812053
hg1912053
hg1812053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1064545
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603776
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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