A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602082



Internal ID16389491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32017810..32023173hg38UCSC Ensembl
Innerchr6:31985587..31990950hg19UCSC Ensembl
Innerchr6:32093565..32098928hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385364
hg195364
hg185364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10480n54
Supporting Variantsnssv1053863
Samples
Known GenesC4A, C4B, C4B_2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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