A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602547



Internal ID16389956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32556447..32558420hg38UCSC Ensembl
Innerchr6:32524224..32526197hg19UCSC Ensembl
Innerchr6:32632202..32634175hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381974
hg191974
hg181974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055849, nssv1055851, nssv1055850, nssv1055848, nssv1055852, nssv1055847
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602547
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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