A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001649



Internal ID68703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113493104..113493104hg38UCSC Ensembl
chr7:113133159..113133159hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541656
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001649
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.038165


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