A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1006499



Internal ID16300455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131038446..131442599hg38UCSC Ensembl
Innerchr4:131959601..132363754hg19UCSC Ensembl
Innerchr4:132179051..132583204hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38404154
hg19404154
hg18404154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595431
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)nssv1006499
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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