A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143181



Internal ID20710221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20096537..20101224hg38UCSC Ensembl
chr6:20096768..20101455hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384688
hg194688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398691
Supporting Variants
Samples
Known GenesMBOAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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