A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483115



Internal ID15582228
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 StatusM
Merged Variants
Supporting Variantsnssv2996256, nssv2996544, nssv2996064, nssv2996200, nssv2996320
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483115
Frequency
Sample Size39
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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