A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143182



Internal ID20710222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20120089..20211716hg38UCSC Ensembl
chr6:20120320..20211947hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3891628
hg1991628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404342
Supporting Variants
Samples
Known GenesMBOAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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