A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402583



Internal ID21060136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160000688..160003418hg38UCSC Ensembl
chr5:159427695..159430425hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382731
hg192731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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