A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505692



Internal ID20878965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65140149..65140931hg38UCSC Ensembl
chr15:65432487..65433269hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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