A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932601



Internal ID22446
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 StatusS
Merged Variantsnsv5562209
Supporting Variants
Samples
Known GenesEXOG, SCN5A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932601
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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