A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519176



Internal ID21843535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190340695..190342632hg38UCSC Ensembl
chr1:190309825..190311762hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981995
Supporting Variants
Samples
Known GenesBRINP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519176
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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