A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483077



Internal ID15582190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164117088..164265951hg38UCSC Ensembl
Innerchr3:163834876..163983739hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38148864
hg19148864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996454
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483077
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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