A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602081



Internal ID16389490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32017441..32038945hg38UCSC Ensembl
Innerchr6:31985218..32006722hg19UCSC Ensembl
Innerchr6:32093196..32114701hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3821505
hg1921505
hg1821506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10482n54
Supporting Variantsnssv1053862
Samples
Known GenesC4A, C4B, C4B_2, CYP21A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602081
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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