A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536426



Internal ID21860781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109077344..109082000hg38UCSC Ensembl
chr1:109619966..109624622hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg384657
hg194657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980589
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536426
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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