A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531212



Internal ID18829493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:78500300..78560532hg38UCSC Ensembl
Innerchr14:78966643..79026875hg19UCSC Ensembl
Innerchr14:78036396..78096628hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3860233
hg1960233
hg1860233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037999
Supporting Variants
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)nssv3531212
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer