A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524747



Internal ID21849105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220636594..220636594hg38UCSC Ensembl
chr1:220809936..220809936hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044688
Supporting Variants
Samples
Known GenesMARK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524747
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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