A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750844



Internal ID20526704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2019178..2019178hg38UCSC Ensembl
chr1:1950617..1950617hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750844
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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