A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996486



Internal ID15581987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160051531..160223194hg38UCSC Ensembl
Innerchr4:160972683..161144346hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38171664
hg19171664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483096
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996486
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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