A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434969



Internal ID213629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84650355..84653734hg38UCSC Ensembl
chr3:84699506..84702885hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg383380
hg193380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935938
Samples
Known GenesLINC00971
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434969
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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