A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698525



Internal ID15435177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19133714..19170744hg38UCSC Ensembl
Innerchr13:19707854..19744884hg19UCSC Ensembl
Innerchr13:18605854..18642884hg18UCSC Ensembl
Innerchr13:18605854..18642884hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3837031
hg1937031
hg1837031
hg1737031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522870
Supporting Variants
Samples
Known GenesRNU6-52P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698525
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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