A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605235



Internal ID16392644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164693974..164800526hg38UCSC Ensembl
Innerchr6:165115007..165214015hg19UCSC Ensembl
Innerchr6:165034997..165134005hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38106553
hg1999009
hg1899009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11034n54
Supporting Variantsnssv1075780
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605235
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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