A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756236



Internal ID20532096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33393725..33393725hg38UCSC Ensembl
chr1:33859326..33859326hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756236
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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