A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519991



Internal ID20893352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70326801..70328100hg38UCSC Ensembl
chr18:67994037..67995336hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042735
Samples
Known GenesSOCS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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