A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139929



Internal ID339119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197696678..197696765hg38UCSC Ensembl
chr3:197423549..197423636hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943850
Samples
Known GenesKIAA0226
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139929
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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