A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982445



Internal ID21891788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210372752..210375180hg38UCSC Ensembl
chr1:210546096..210548524hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526433
Samples
Known GenesHHAT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982445
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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