A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952840



Internal ID16955027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:51846583..51949982hg38UCSC Ensembl
Outerchr14:52313301..52416700hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38103400
hg19103400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998341
SamplesBILGI_BIOE
Known GenesGNG2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952840
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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