A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482918



Internal ID260363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48676996..49241090hg38UCSC Ensembl
chr10:49885041..50449135hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38564095
hg19564095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035089
Samples
Known GenesC10orf128, FAM170B, FAM170B-AS1, LRRC18, MIR4294, VSTM4, WDFY4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482918
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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