A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532366



Internal ID21856722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207581221..207581335hg38UCSC Ensembl
chr1:207754566..207754680hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982356
Supporting Variants
Samples
Known GenesCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532366
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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