A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562209



Internal ID335168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38502175..38676379hg38UCSC Ensembl
chr3:38543666..38717870hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38174205
hg19174205
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932601
Samples
Known GenesEXOG, SCN5A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562209
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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