A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143934



Internal ID343136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69194754..69194824hg38UCSC Ensembl
chr10:70954510..70954580hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035103
Samples
Known GenesSUPV3L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143934
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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