A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532763



Internal ID20906124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58689501..58693011hg38UCSC Ensembl
chr18:56356733..56360243hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg383511
hg193511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042342
Samples
Known GenesMALT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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