A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487132



Internal ID21144685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68312801..68314600hg38UCSC Ensembl
chr14:68779518..68781317hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020560
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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