A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820095



Internal ID16114051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112182341..112205515hg38UCSC Ensembl
Innerchr13:112836655..112859829hg19UCSC Ensembl
Innerchr13:111884656..111907830hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3823175
hg1923175
hg1823175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563194
Supporting Variants
Samples
Known GenesLINC01070
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820095
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