A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048662



Internal ID21957896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177066910..177066910hg38UCSC Ensembl
chr2:177931638..177931638hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048662
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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