A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530388



Internal ID21854744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58981127..58981276hg38UCSC Ensembl
chr1:59446799..59446948hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530388
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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