A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517542



Internal ID21841901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234651003..234651077hg38UCSC Ensembl
chr1:234786749..234786823hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517542
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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