A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602034



Internal ID16042757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31991487..32002199hg38UCSC Ensembl
Innerchr6:31959264..31969976hg19UCSC Ensembl
Innerchr6:32067243..32077954hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3810713
hg1910713
hg1810712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053725
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)nsv602034
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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