A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561511



Internal ID334489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142847112..142847120hg38UCSC Ensembl
chr7:142544875..142544883hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561511
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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