A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2763074



Internal ID17792850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76886304..76894908hg38UCSC Ensembl
Innerchr14:77352647..77361251hg19UCSC Ensembl
Innerchr14:76422400..76431004hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg388605
hg198605
hg188605
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977490
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2763074
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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