A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982682



Internal ID21892025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2285526..2296232hg38UCSC Ensembl
chr1:2216965..2227671hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3810707
hg1910707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535883
Samples
Known GenesSKI
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982682
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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