A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429920



Internal ID208751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21786598..21794877hg38UCSC Ensembl
chr1:22113091..22121370hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg388280
hg198280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429920
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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