A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532602



Internal ID21856958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224192205..224192205hg38UCSC Ensembl
chr1:224379907..224379907hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044893
Supporting Variants
Samples
Known GenesDEGS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532602
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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