A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489091



Internal ID266380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135234584..135235749hg38UCSC Ensembl
chr7:134919336..134920501hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003680
Samples
Known GenesSTRA8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489091
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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