A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519951



Internal ID15100558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96269937..96271261hg38UCSC Ensembl
Innerchr13:96922191..96923515hg19UCSC Ensembl
Innerchr13:95720192..95721516hg18UCSC Ensembl
Innerchr13:95720192..95721516hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381325
hg191325
hg181325
hg171325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690441, nssv687171, nssv676172, nssv659607
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519951
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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