A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143457



Internal ID342658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96914319..96925222hg38UCSC Ensembl
chr10:98674076..98684979hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3810904
hg1910904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036634
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143457
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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