A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749008



Internal ID20525036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225676773..225676836hg38UCSC Ensembl
chr1:225864475..225864538hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749008
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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