A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602770



Internal ID16390179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32645970..32658394hg38UCSC Ensembl
Innerchr6:32613747..32626171hg19UCSC Ensembl
Innerchr6:32721725..32734149hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812425
hg1912425
hg1812425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10595n54
Supporting Variantsnssv1056837, nssv1056838, nssv1056836
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602770
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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