A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531092



Internal ID18482687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66586328..66654023hg38UCSC Ensembl
Innerchr14:67053046..67120741hg19UCSC Ensembl
Innerchr14:66122799..66190494hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3867696
hg1967696
hg1867696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048504
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)nssv3531092
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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