A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602401



Internal ID16389810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32517715..32553474hg38UCSC Ensembl
Innerchr6:32485492..32521251hg19UCSC Ensembl
Innerchr6:32593470..32629229hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3835760
hg1935760
hg1835760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10526n54
Supporting Variantsnssv1055386
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602401
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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