A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv809977



Internal ID16103933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:44163056..44218986hg38UCSC Ensembl
Innerchr13:44737192..44793122hg19UCSC Ensembl
Innerchr13:43635192..43691122hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3855931
hg1955931
hg1855931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561574
Supporting Variants
Samples
Known GenesMIR8079
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv809977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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