A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498273



Internal ID20871482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40725770..40726795hg38UCSC Ensembl
chr15:41017968..41018993hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024216
Samples
Known GenesRAD51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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