A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996419



Internal ID15581920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80731169..80894887hg38UCSC Ensembl
Innerchr13:81305304..81469022hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38163719
hg19163719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483091
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996419
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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