A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601248



Internal ID16388657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29908663hg38UCSC Ensembl
Innerchr6:29851443..29876440hg19UCSC Ensembl
Innerchr6:29959422..29984419hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3824998
hg1924998
hg1824998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10345n54
Supporting Variantsnssv1051740
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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