A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562978



Internal ID16350387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102191639..102211595hg38UCSC Ensembl
Innerchr13:102843989..102863945hg19UCSC Ensembl
Innerchr13:101641990..101661946hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3819957
hg1919957
hg1819957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818818
Samples
Known GenesFGF14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562978
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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