A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062815



Internal ID21972048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10681921..10681921hg38UCSC Ensembl
chr5:10682033..10682033hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537867
Samples
Known GenesDAP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062815
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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