A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742275



Internal ID20518257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221498880..221501366hg38UCSC Ensembl
chr1:221672222..221674708hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382487
hg192487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742275
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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