A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486121



Internal ID263495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138678043..138691761hg38UCSC Ensembl
chr7:138362788..138376506hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3813719
hg1913719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006276
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486121
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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