A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537099



Internal ID21861454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118712023..118718464hg38UCSC Ensembl
chr1:119254646..119261087hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg386442
hg196442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537099
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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