A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140125



Internal ID339317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:198169574..198235000hg38UCSC Ensembl
chr3:197896445..197961871hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3865427
hg1965427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945284
Samples
Known GenesFAM157A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140125
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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