A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051980



Internal ID18794511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66609288..66673564hg38UCSC Ensembl
Innerchr14:67076006..67140282hg19UCSC Ensembl
Innerchr14:66145759..66210035hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3864277
hg1964277
hg1864277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531101
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)nsv1051980
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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