A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519476



Internal ID21843835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75869952..75870290hg38UCSC Ensembl
chr2:76097078..76097416hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519476
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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