A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519296



Internal ID15446589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99575214..99577222hg38UCSC Ensembl
Innerchr13:100227468..100229476hg19UCSC Ensembl
Innerchr13:99025469..99027477hg18UCSC Ensembl
Innerchr13:99025469..99027477hg17UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg382009
hg192009
hg182009
hg172009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672655, nssv656247, nssv655231
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519296
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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