A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519146



Internal ID21843505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202624533..202624588hg38UCSC Ensembl
chr1:202593661..202593716hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982333
Supporting Variants
Samples
Known GenesSYT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519146
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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