A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv818818



Internal ID16112774
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 StatusS
Merged Variantsnsv562978
Supporting Variants
Samples
Known GenesFGF14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv818818
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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