A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036894



Internal ID92352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91384463..91384495hg38UCSC Ensembl
chr10:93144220..93144252hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534999
Supporting Variants
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036894
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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