A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555296



Internal ID328457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25586437..25586487hg38UCSC Ensembl
chr7:25626057..25626107hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382313
hg192313
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555296
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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