A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989004



Internal ID60093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149668104..149674273hg38UCSC Ensembl
chr6:149989240..149995409hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386170
hg196170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455130
Supporting Variants
Samples
Known GenesLATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989004
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007027


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