A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531098



Internal ID18482693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66592552..66654023hg38UCSC Ensembl
Innerchr14:67059270..67120741hg19UCSC Ensembl
Innerchr14:66129023..66190494hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3861472
hg1961472
hg1861472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046627
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)nssv3531098
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