A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483125



Internal ID15235599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82448179..82617091hg38UCSC Ensembl
Innerchr15:83116860..83285842hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38168913
hg19168983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996511, nssv2996392
Samples
Known GenesCPEB1, CSPG4P8, LOC727751, LOC80154, RPS17, RPS17L
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483125
Frequency
Sample Size39
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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