A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039403



Internal ID19128622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98326581..98433392hg38UCSC Ensembl
Innerchr13:98978835..99085646hg19UCSC Ensembl
Innerchr13:97776836..97883647hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38106812
hg19106812
hg18106812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525522
Samples
Known GenesFARP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039403
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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