A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668306



Internal ID15058272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98439380..98463263hg38UCSC Ensembl
Innerchr13:99091634..99115517hg19UCSC Ensembl
Innerchr13:97889635..97913518hg18UCSC Ensembl
Innerchr13:97889635..97913518hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3823884
hg1923884
hg1823884
hg1723884
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517409
Supporting Variants
Samples
Known GenesFARP1, STK24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668306
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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