A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604914



Internal ID16392323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153238742..153293797hg38UCSC Ensembl
Innerchr6:153559877..153614932hg19UCSC Ensembl
Innerchr6:153601570..153656625hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3855056
hg1955056
hg1855056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074597
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604914
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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