A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147272



Internal ID346454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178207687..178214532hg38UCSC Ensembl
chr3:177925475..177932320hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg386846
hg196846
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147272
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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