A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984962



Internal ID21894305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84677087..84859877hg38UCSC Ensembl
chr1:85142770..85325560hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38182791
hg19182791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524036
Samples
Known GenesLPAR3, SSX2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984962
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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