A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670834



Internal ID15060800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96788383..96797067hg38UCSC Ensembl
Innerchr13:97440637..97449321hg19UCSC Ensembl
Innerchr13:96238638..96247322hg18UCSC Ensembl
Innerchr13:96238638..96247322hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg388685
hg198685
hg188685
hg178685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516784
Supporting Variants
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670834
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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