A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602537



Internal ID16389946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32555036..32556447hg38UCSC Ensembl
Innerchr6:32522813..32524224hg19UCSC Ensembl
Innerchr6:32630791..32632202hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381412
hg191412
hg181412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10556n54
Supporting Variantsnssv1055810, nssv1055817, nssv1055822, nssv1055807, nssv1055811, nssv1055819, nssv1055818, nssv1055815, nssv1055809, nssv1055821, nssv1055808, nssv1055812, nssv1055813, nssv1055814, nssv1055820, nssv1055816
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602537
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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