A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516784



Internal ID15097391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96788317..96797067hg38UCSC Ensembl
Innerchr13:97440571..97449321hg19UCSC Ensembl
Innerchr13:96238572..96247322hg18UCSC Ensembl
Innerchr13:96238572..96247322hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg388751
hg198751
hg188751
hg178751
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691535, nssv670834, nssv677384, nssv689079
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516784
Frequency
Sample Size2026
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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