A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009394



Internal ID16303350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148444722..148445719hg38UCSC Ensembl
Innerchr4:149365874..149366871hg19UCSC Ensembl
Innerchr4:149585324..149586321hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38998
hg19998
hg18998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595681
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)nssv1009394
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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