A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933150



Internal ID22826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64997568..65003524hg38UCSC Ensembl
chr3:64983243..64989199hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg385957
hg195957
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560200
Supporting Variants
Samples
Known GenesADAMTS9-AS2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933150
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.074305


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