A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054762



Internal ID21963996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76556976..76556976hg38UCSC Ensembl
chr2:76784102..76784102hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054762
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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