A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603639



Internal ID16044362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:70885448..70913550hg38UCSC Ensembl
Innerchr6:71595151..71623253hg19UCSC Ensembl
Innerchr6:71651872..71679974hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3828103
hg1928103
hg1828103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1063665, nssv1063664
Samples
Known GenesB3GAT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603639
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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