A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745889



Internal ID21387849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225950733..225952920hg38UCSC Ensembl
chr1:226138433..226140620hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg382188
hg192188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433058
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745889
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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