A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531099



Internal ID18482694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66592552..66656921hg38UCSC Ensembl
Innerchr14:67059270..67123639hg19UCSC Ensembl
Innerchr14:66129023..66193392hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3864370
hg1964370
hg1864370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049050
Supporting Variants
Samples
Known GenesGPHN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531099
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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