A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036092



Internal ID91806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49874368..50014368hg38UCSC Ensembl
chr10:51082414..51774128hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38140001
hg19691715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479740
Supporting Variants
Samples
Known GenesAGAP6, AGAP7, AGAP8, LOC728407, MSMB, NCOA4, PARG, TIMM23
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036092
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004558


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