A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604532



Internal ID16391941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113750518..113792854hg38UCSC Ensembl
Innerchr6:114071720..114114057hg19UCSC Ensembl
Innerchr6:114178413..114220750hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3842337
hg1942338
hg1842338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154874
Samples1780862373_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604532
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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