A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523746



Internal ID21848105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37942306..37942781hg38UCSC Ensembl
chr1:38407978..38408453hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984214
Supporting Variants
Samples
Known GenesINPP5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523746
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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