A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745554



Internal ID20521564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151599280..151599522hg38UCSC Ensembl
chr1:151571756..151571998hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745554
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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