A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285611



Internal ID20494829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141703339..141703339hg38UCSC Ensembl
chr7:141403139..141403139hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385876
hg195876
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285611
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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