A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984572



Internal ID21893915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44139072..44139403hg38UCSC Ensembl
chr1:44604744..44605075hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984572
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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