A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603476



Internal ID16390885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65926311..66009704hg38UCSC Ensembl
Innerchr6:66636204..66719597hg19UCSC Ensembl
Innerchr6:66692925..66776318hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3883394
hg1983394
hg1883394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153717
SamplesHGDP00562
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603476
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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