A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981100



Internal ID21890443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145176860..145176953hg38UCSC Ensembl
chr1:149664413..149664506hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530634
Samples
Known GenesLINC00869
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981100
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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