A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834920



Internal ID16128876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474444..105475189hg38UCSC Ensembl
Innerchr14:105940781..105941526hg19UCSC Ensembl
Innerchr14:105011826..105012571hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38746
hg19746
hg18746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566257
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)nssv834920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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