A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604168



Internal ID16391577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94046342..94257296hg38UCSC Ensembl
Innerchr6:94756060..94967014hg19UCSC Ensembl
Innerchr6:94812781..95023735hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38210955
hg19210955
hg18210955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1068423
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604168
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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