A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375726



Internal ID21033279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17237001..17243900hg38UCSC Ensembl
chr5:17237110..17244009hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130232
Samples
Known GenesBASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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