A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526499



Internal ID21850857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201210972..201210972hg38UCSC Ensembl
chr1:201180100..201180100hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059456
Supporting Variants
Samples
Known GenesIGFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526499
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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