A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981429



Internal ID21890772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16142768..16142889hg38UCSC Ensembl
chr1:16469263..16469384hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530022
Samples
Known GenesEPHA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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