A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411058



Internal ID21068611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102660694..102663670hg38UCSC Ensembl
chr5:101996398..101999374hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg382977
hg192977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122115
Samples
Known GenesLINC00491
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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