A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459158



Internal ID237176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13930573..13931065hg38UCSC Ensembl
chr7:13970198..13970690hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993049
Samples
Known GenesETV1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459158
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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