A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602021



Internal ID16042744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31986316..31989791hg38UCSC Ensembl
Innerchr6:31954093..31957568hg19UCSC Ensembl
Innerchr6:32062072..32065547hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383476
hg193476
hg183476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10473n54
Supporting Variantsnssv1053684, nssv1053685
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)nsv602021
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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