A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604098



Internal ID16391507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85881484..85965782hg38UCSC Ensembl
Innerchr6:86591202..86675500hg19UCSC Ensembl
Innerchr6:86647921..86732219hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3884299
hg1984299
hg1884299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10830n54
Supporting Variantsnssv1067384, nssv1067383
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604098
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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