A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492105



Internal ID269326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99517361..99519530hg38UCSC Ensembl
chr7:99114984..99117153hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382170
hg192170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002900
Samples
Known GenesZKSCAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492105
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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