A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532580



Internal ID18484175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89882005..89968468hg38UCSC Ensembl
Innerchr14:90348349..90434812hg19UCSC Ensembl
Innerchr14:89418102..89504565hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3886464
hg1986464
hg1886464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045864
Supporting Variants
Samples
Known GenesEFCAB11, TDP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3532580
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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