A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604838



Internal ID16045561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145388235..145520010hg38UCSC Ensembl
Innerchr6:145709371..145841146hg19UCSC Ensembl
Innerchr6:145751064..145882839hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38131776
hg19131776
hg18131776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074344
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604838
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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