A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562379



Internal ID335336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36978157..36985404hg38UCSC Ensembl
chr3:37019648..37026895hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387248
hg197248
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562379
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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