A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602206



Internal ID16389615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32490550..32538126hg38UCSC Ensembl
Innerchr6:32458327..32505903hg19UCSC Ensembl
Innerchr6:32566305..32613881hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3847577
hg1947577
hg1847577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10502n54
Supporting Variantsnssv1054590, nssv1054586, nssv1054589, nssv1054584, nssv1054588, nssv1054585, nssv1054587
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602206
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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