A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601978



Internal ID16042701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31982489..31989587hg38UCSC Ensembl
Innerchr6:31950266..31957364hg19UCSC Ensembl
Innerchr6:32058245..32065343hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg387099
hg197099
hg187099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10467n54
Supporting Variantsnssv1053578, nssv1053577
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)nsv601978
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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