A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525671



Internal ID21850029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31411249..31417285hg38UCSC Ensembl
chr1:31884096..31890132hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg386037
hg196037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984010
Supporting Variants
Samples
Known GenesSERINC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525671
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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