A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139177



Internal ID338361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36525504..36525574hg38UCSC Ensembl
chr3:36566996..36567066hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932562
Samples
Known GenesSTAC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139177
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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