A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419801



Internal ID198924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160984047..160990908hg38UCSC Ensembl
chr1:160953837..160960698hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg386862
hg196862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16892346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419801
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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