A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562868



Internal ID16003591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98303535..98556312hg38UCSC Ensembl
Innerchr13:98955789..99208566hg19UCSC Ensembl
Innerchr13:97753790..98006567hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38252778
hg19252778
hg18252778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149454
SamplesHGDP01081
Known GenesFARP1, STK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562868
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer