A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996256



Internal ID15581757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170202461..170366806hg38UCSC Ensembl
Innerchr4:171123612..171287957hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38164346
hg19164346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483115
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996256
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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