A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834848



Internal ID16128804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474226..105475085hg38UCSC Ensembl
Innerchr14:105940563..105941422hg19UCSC Ensembl
Innerchr14:105011608..105012467hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38860
hg19860
hg18860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566231
Supporting Variants
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834848
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