A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036093



Internal ID91807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49884368..49929368hg38UCSC Ensembl
chr10:51092414..51358990hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3845001
hg19266577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489872
Supporting Variants
Samples
Known GenesAGAP8, LOC728407, PARG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036093
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009248


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