A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604842



Internal ID16392251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148288264..148329728hg38UCSC Ensembl
Innerchr6:148609400..148650864hg19UCSC Ensembl
Innerchr6:148651093..148692557hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3841465
hg1941465
hg1841465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155790
Samples1780862573_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604842
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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