A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896798



Internal ID172013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226169708..226173774hg38UCSC Ensembl
chr1:226357409..226361475hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg384067
hg194067
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556176
Supporting Variants
Samples
Known GenesACBD3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896798
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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