A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482281



Internal ID259739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99063232..99063286hg38UCSC Ensembl
chr7:98660855..98660909hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000716
Samples
Known GenesSMURF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482281
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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