A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057575



Internal ID21966808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11468069..11468069hg38UCSC Ensembl
chr2:11608195..11608195hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382730
hg192730
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057575
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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