A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036891



Internal ID92350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91362802..91362853hg38UCSC Ensembl
chr10:93122559..93122610hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5411985
Supporting Variants
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036891
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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