A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517907



Internal ID15098514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96684993..96739966hg38UCSC Ensembl
Innerchr13:97337247..97392220hg19UCSC Ensembl
Innerchr13:96135248..96190221hg18UCSC Ensembl
Innerchr13:96135248..96190221hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3854974
hg1954974
hg1854974
hg1754974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694059
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517907
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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