A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143527



Internal ID342728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119522368..119546368hg38UCSC Ensembl
chr10:121281880..121305880hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3824001
hg1924001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688327
Samples
Known GenesRGS10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143527
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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