A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036384



Internal ID92003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89035037..89042487hg38UCSC Ensembl
chr10:90794794..90802244hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg387451
hg197451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036384
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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