A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009393



Internal ID16303349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148444722..148445537hg38UCSC Ensembl
Innerchr4:149365874..149366689hg19UCSC Ensembl
Innerchr4:149585324..149586139hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38816
hg19816
hg18816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595680
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)nssv1009393
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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