A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490653



Internal ID21148206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68126325..68137109hg38UCSC Ensembl
chr14:68593042..68603826hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3810785
hg1910785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020549
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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