A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829639



Internal ID16123595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:79041973..79089308hg38UCSC Ensembl
Innerchr14:79508316..79555651hg19UCSC Ensembl
Innerchr14:78578069..78625404hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3847336
hg1947336
hg1847336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565247
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)nssv829639
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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