A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688464



Internal ID15078430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98439380..98448293hg38UCSC Ensembl
Innerchr13:99091634..99100547hg19UCSC Ensembl
Innerchr13:97889635..97898548hg18UCSC Ensembl
Innerchr13:97889635..97898548hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg388914
hg198914
hg188914
hg178914
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517409
Supporting Variants
Samples
Known GenesFARP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688464
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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