A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751359



Internal ID20527220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56929077..56929077hg38UCSC Ensembl
chr1:57394750..57394750hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751359
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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