A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996492



Internal ID15581993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103437775..103576897hg38UCSC Ensembl
Innerchr4:104358932..104498054hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38139123
hg19139123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483011
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996492
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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