A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443326



Internal ID221727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216876934..216884105hg38UCSC Ensembl
chr1:217050276..217057447hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg387172
hg197172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897095
Samples
Known GenesESRRG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443326
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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