A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941951



Internal ID21362023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102379630..102379681hg38UCSC Ensembl
chr14:102845967..102846018hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183357
SamplesHG002
Known GenesTECPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941951
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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