A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834806



Internal ID15782076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105458373..105474172hg38UCSC Ensembl
Innerchr14:105924710..105940509hg19UCSC Ensembl
Innerchr14:104995755..105011554hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3815800
hg1915800
hg1815800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566207
Supporting Variants
Samples
Known GenesCRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834806
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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