A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929934



Internal ID21350004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76231974..76231974hg38UCSC Ensembl
chr14:76698317..76698317hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194872
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929934
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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