A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604321



Internal ID16391730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102071070..102155138hg38UCSC Ensembl
Innerchr6:102518945..102603013hg19UCSC Ensembl
Innerchr6:102625638..102709706hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3884069
hg1984069
hg1884069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1070796
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604321
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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