A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602168



Internal ID16389577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32544387hg38UCSC Ensembl
Innerchr6:32455482..32512164hg19UCSC Ensembl
Innerchr6:32563460..32620142hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3856683
hg1956683
hg1856683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10502n54
Supporting Variantsnssv1054446, nssv1054447
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602168
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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