A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980568



Internal ID21889911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10576554..10583990hg38UCSC Ensembl
chr1:10636611..10644047hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387437
hg197437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534121
Samples
Known GenesPEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980568
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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