A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926645



Internal ID21346714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24212556..24212556hg38UCSC Ensembl
chr14:24681762..24681762hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195063
SamplesHG002
Known GenesCHMP4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926645
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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