A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983970



Internal ID18272475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77119831..77126424hg38UCSC Ensembl
Innerchr14:77586174..77592767hg19UCSC Ensembl
Innerchr14:76655927..76662520hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg386594
hg196594
hg186594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758400
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983970
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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