A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981418



Internal ID21890761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158292136..158301456hg38UCSC Ensembl
chr1:158261926..158271246hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389321
hg199321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521313
Samples
Known GenesCD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981418
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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