A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602498



Internal ID16389907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32551331..32554371hg38UCSC Ensembl
Innerchr6:32519108..32522148hg19UCSC Ensembl
Innerchr6:32627086..32630126hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383041
hg193041
hg183041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10548n54
Supporting Variantsnssv1055703, nssv1055704
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602498
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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