A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601055



Internal ID16388464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18698911..19116208hg38UCSC Ensembl
Innerchr6:18699142..19116439hg19UCSC Ensembl
Innerchr6:18807121..19224418hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38417298
hg19417298
hg18417298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10311n54
Supporting Variantsnssv1154186
Samples1780862347_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601055
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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