A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601455



Internal ID16388864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29941743..29949726hg38UCSC Ensembl
Innerchr6:29909520..29917503hg19UCSC Ensembl
Innerchr6:30017499..30025482hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg387984
hg197984
hg187984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10364n54
Supporting Variantsnssv1052231
Samples
Known GenesHLA-A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601455
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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