A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976845



Internal ID18612051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77155522..77182848hg38UCSC Ensembl
Innerchr14:77621865..77649191hg19UCSC Ensembl
Innerchr14:76691618..76718944hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827327
hg1927327
hg1827327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762337
SamplesHGDP00998
Known GenesTMEM63C
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976845
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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