A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738545



Internal ID20514515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182741613..182741741hg38UCSC Ensembl
chr1:182710748..182710876hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738545
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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