A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536221



Internal ID21860576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43098961..43098961hg38UCSC Ensembl
chr2:43326099..43326099hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041528
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536221
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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