A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605182



Internal ID16045905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162745870..162859172hg38UCSC Ensembl
Innerchr6:163166902..163280204hg19UCSC Ensembl
Innerchr6:163086892..163200194hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38113303
hg19113303
hg18113303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075578
Samples
Known GenesPACRG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605182
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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