A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422583



Internal ID201625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3821016..4289147hg38UCSC Ensembl
chr1:3737580..4349207hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38468132
hg19611628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903269
Samples
Known GenesC1orf174, CEP104, DFFB, LINC01134, LOC728716
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422583
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer