A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829609



Internal ID16123565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:78511838..78561161hg38UCSC Ensembl
Innerchr14:78978181..79027504hg19UCSC Ensembl
Innerchr14:78047934..78097257hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3849324
hg1949324
hg1849324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565235
Supporting Variants
Samples
Known GenesNRXN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829609
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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