A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065425



Internal ID21974658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156941031..156941031hg38UCSC Ensembl
chr7:156733725..156733725hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065425
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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