A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143368



Internal ID342569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133197130..133249130hg38UCSC Ensembl
chr10:135010634..135062634hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3852001
hg1952001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043458
Samples
Known GenesKNDC1, MIR202, MIR202HG, UTF1, VENTX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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