A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036811



Internal ID92293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87284368..87454368hg38UCSC Ensembl
chr10:89044125..89214125hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38170001
hg19170001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143585
Supporting Variants
Samples
Known GenesLINC00864, LOC439994, NUTM2A-AS1, NUTM2D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036811
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000962


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