A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062623



Internal ID21971856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53617231..53617231hg38UCSC Ensembl
chr7:53684924..53684924hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062623
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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