A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427079



Internal ID205992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35429523..35431934hg38UCSC Ensembl
chr1:35895124..35897535hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382412
hg192412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427079
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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