A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834834



Internal ID16128790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474172..105475136hg38UCSC Ensembl
Innerchr14:105940509..105941473hg19UCSC Ensembl
Innerchr14:105011554..105012518hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38965
hg19965
hg18965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566225
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)nssv834834
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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