A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982176



Internal ID21891519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1741975..1742296hg38UCSC Ensembl
chr1:1673414..1673735hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519664
Samples
Known GenesSLC35E2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982176
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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