A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996074



Internal ID15581575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:82939864..83104819hg38UCSC Ensembl
Innerchr13:83513999..83678954hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38164956
hg19164956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483101
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996074
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer