A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183844



Internal ID21322640
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948710
Supporting Variants
SamplesHG002
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183844
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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