A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541100



Internal ID315747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55445165..55445202hg38UCSC Ensembl
chr7:55512858..55512895hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541100
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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