A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429271



Internal ID208121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55272692..55297413hg38UCSC Ensembl
chr1:55738365..55763086hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3824722
hg1924722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429271
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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