A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602939



Internal ID16390348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35790295..35815720hg38UCSC Ensembl
Innerchr6:35758072..35783497hg19UCSC Ensembl
Innerchr6:35866050..35891475hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3825426
hg1925426
hg1825426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058367
Samples
Known GenesCLPS, LHFPL5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602939
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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