A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057045



Internal ID21966281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195587115..195587115hg38UCSC Ensembl
chr2:196451839..196451839hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057045
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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