A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974480



Internal ID18609691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100634902..100661964hg38UCSC Ensembl
Innerchr14:101101239..101128301hg19UCSC Ensembl
Innerchr14:100170992..100198054hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3827063
hg1927063
hg1827063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765705
SamplesHGDP00998
Known GenesLINC00523
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974480
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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