A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980688



Internal ID21890031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100166120..100166905hg38UCSC Ensembl
chr1:100631676..100632461hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517878
Samples
Known GenesLRRC39
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980688
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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