A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419282



Internal ID198418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32400837..32403991hg38UCSC Ensembl
chr1:32866438..32869592hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg383155
hg193155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419282
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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