A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899338



Internal ID332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20372641..20372913hg38UCSC Ensembl
chr1:20699134..20699406hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427757
Supporting Variants
Samples
Known GenesLINC01141
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899338
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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