A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996532



Internal ID15582033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34775701..34925104hg38UCSC Ensembl
Innerchr4:34777323..34926726hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38149404
hg19149404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483095
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996532
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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