A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536829



Internal ID21861184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6025922..6025922hg38UCSC Ensembl
chr2:6166054..6166054hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044097
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536829
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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