A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522959



Internal ID21847318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52636114..52636246hg38UCSC Ensembl
chr1:53101786..53101918hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984424
Supporting Variants
Samples
Known GenesFAM159A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522959
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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