A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433057



Internal ID21395059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225950724..225952899hg38UCSC Ensembl
chr1:226138424..226140599hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv51n172
Supporting Variantsnssv15751577
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433057
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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