A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892097



Internal ID168922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167913656..167913730hg38UCSC Ensembl
chr1:167882894..167882968hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417773
Supporting Variants
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01842


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