A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397660



Internal ID21055213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152638537..152639048hg38UCSC Ensembl
chr5:152018097..152018608hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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