A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602221



Internal ID16389630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32490550..32626497hg38UCSC Ensembl
Innerchr6:32458327..32594274hg19UCSC Ensembl
Innerchr6:32566305..32702252hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38135948
hg19135948
hg18135948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10497n54
Supporting Variantsnssv1054620, nssv1054619, nssv1054625, nssv1054624, nssv1054618, nssv1054621, nssv1054622, nssv1054623
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602221
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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