A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004453



Internal ID70604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141703339..141703339hg38UCSC Ensembl
chr7:141403139..141403139hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385992
hg195992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541061
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004453
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.100599


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