A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740937



Internal ID20516914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36688482..36688797hg38UCSC Ensembl
chr1:37154083..37154398hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740937
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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