A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504107



Internal ID20877367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67374520..67377457hg38UCSC Ensembl
chr16:67408423..67411360hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382938
hg192938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031350
Samples
Known GenesLRRC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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