A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521410



Internal ID15102017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96253363..96256468hg38UCSC Ensembl
Innerchr13:96905617..96908722hg19UCSC Ensembl
Innerchr13:95703618..95706723hg18UCSC Ensembl
Innerchr13:95703618..95706723hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg383106
hg193106
hg183106
hg173106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698020
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521410
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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