A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530960



Internal ID21855316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:194584956..194588894hg38UCSC Ensembl
chr2:195449680..195453618hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg383939
hg193939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530960
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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