A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603080



Internal ID16390489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49351360..49409211hg38UCSC Ensembl
Innerchr6:49319025..49376924hg19UCSC Ensembl
Innerchr6:49426984..49484883hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3857852
hg1957900
hg1857900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153704
Samples1798860114_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603080
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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