A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037112



Internal ID19126331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:78946112..79061313hg38UCSC Ensembl
Innerchr14:79412455..79527656hg19UCSC Ensembl
Innerchr14:78482208..78597409hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38115202
hg19115202
hg18115202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713532
Samples
Known GenesNRXN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037112
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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