A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565237



Internal ID16352646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:78690697..78699265hg38UCSC Ensembl
Innerchr14:79157040..79165608hg19UCSC Ensembl
Innerchr14:78226793..78235361hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg388569
hg198569
hg188569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3787n54
Supporting Variantsnssv829611
Samples
Known GenesNRXN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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