A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1006491



Internal ID16300447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131020178..131407059hg38UCSC Ensembl
Innerchr4:131941333..132328214hg19UCSC Ensembl
Innerchr4:132160783..132547664hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38386882
hg19386882
hg18386882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595424
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1006491
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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