A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601682



Internal ID16389091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31315520..31350526hg38UCSC Ensembl
Innerchr6:31283297..31318303hg19UCSC Ensembl
Innerchr6:31391276..31426282hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3835007
hg1935007
hg1835007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10381n54
Supporting Variantsnssv1053050, nssv1053048, nssv1053049
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601682
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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