A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953999



Internal ID21374068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36511607..36511673hg38UCSC Ensembl
chr14:36980812..36980878hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183825
SamplesHG002
Known GenesSFTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953999
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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