A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142414



Internal ID341614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115900222..116094222hg38UCSC Ensembl
chr8:116912447..117106447hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38194001
hg19194001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017913
Samples
Known GenesLINC00536
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142414
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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