A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039369



Internal ID18781900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21030895..21062142hg38UCSC Ensembl
Innerchr14:21499054..21530301hg19UCSC Ensembl
Innerchr14:20568894..20600141hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3831248
hg1931248
hg1831248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532168
Samples
Known GenesNDRG2, RNASE13, RNASE7, RNASE8, TPPP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039369
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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