A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948710



Internal ID21368779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68136314..68137014hg38UCSC Ensembl
chr14:68603031..68603731hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183844
SamplesHG002
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948710
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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