A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526574



Internal ID21850932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108674499..108680424hg38UCSC Ensembl
chr1:109217121..109223046hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385926
hg195926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980729
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526574
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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