A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602938



Internal ID16390347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35790295..35798799hg38UCSC Ensembl
Innerchr6:35758072..35766576hg19UCSC Ensembl
Innerchr6:35866050..35874554hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg388505
hg198505
hg188505
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058366, nssv1058363, nssv1058364, nssv1058365
Samples
Known GenesCLPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602938
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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