A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142686



Internal ID341887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97936779..97942779hg38UCSC Ensembl
chr7:97566091..97572091hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142686
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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