A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17527281



Internal ID21851638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33795087..33795087hg38UCSC Ensembl
chr1:34260688..34260688hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045523
Supporting Variants
Samples
Known GenesCSMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17527281
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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