A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534614



Internal ID21858969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67579750..67579852hg38UCSC Ensembl
chr1:68045433..68045535hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984801
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534614
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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