A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977490



Internal ID18612696
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763074
SamplesHGDP00665
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977490
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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