A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556667



Internal ID329799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133183079..133183130hg38UCSC Ensembl
chr7:132867837..132867888hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556667
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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