A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589572



Internal ID16376981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7036492..7111965hg38UCSC Ensembl
Innerchr3:7078179..7153652hg19UCSC Ensembl
Innerchr3:7053179..7128652hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3875474
hg1975474
hg1875474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8204n54
Supporting Variantsnssv958606
Samples
Known GenesGRM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589572
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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