A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601776



Internal ID16389185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31321494..31370583hg38UCSC Ensembl
Innerchr6:31289271..31338360hg19UCSC Ensembl
Innerchr6:31397250..31446339hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3849090
hg1949090
hg1849090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10411n54
Supporting Variantsnssv1053204
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601776
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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