A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980624



Internal ID21889967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103460838..103460977hg38UCSC Ensembl
chr1:104003460..104003599hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534545
Samples
Known GenesLOC101928436
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980624
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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