A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560925



Internal ID333918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25904010..25904061hg38UCSC Ensembl
chr7:25943630..25943681hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560925
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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