A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400797



Internal ID21058350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150460642..150466316hg38UCSC Ensembl
chr5:149840205..149845879hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg385675
hg195675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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