A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604522



Internal ID16391931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113380690..113381301hg38UCSC Ensembl
Innerchr6:113701892..113702503hg19UCSC Ensembl
Innerchr6:113808585..113809196hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38612
hg19612
hg18612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10912n54
Supporting Variantsnssv1072075
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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