A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952862



Internal ID17301736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:69614984..69625983hg38UCSC Ensembl
Outerchr14:70081701..70092700hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3811000
hg1911000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998365
SamplesBILGI_BIOE
Known GenesKIAA0247
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952862
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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