A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703670



Internal ID15093636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19637294..19824602hg38UCSC Ensembl
Innerchr13:20211434..20398742hg19UCSC Ensembl
Innerchr13:19109434..19296742hg18UCSC Ensembl
Innerchr13:19109434..19296742hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38187309
hg19187309
hg18187309
hg17187309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516945
Supporting Variants
Samples
Known GenesMPHOSPH8, PSPC1, ZMYM5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703670
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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