A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980532



Internal ID21889875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:112660582..112662420hg38UCSC Ensembl
chr1:113203204..113205042hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381839
hg191839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525536
Samples
Known GenesCAPZA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980532
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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