A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531204



Internal ID18482799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75711238..75792533hg38UCSC Ensembl
Innerchr14:76177581..76258876hg19UCSC Ensembl
Innerchr14:75247334..75328629hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3881296
hg1981296
hg1881296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047680
Supporting Variants
Samples
Known GenesTTLL5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531204
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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