A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423461



Internal ID22481331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117317033..117317789hg38UCSC Ensembl
chr6:117638196..117638952hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902919
Supporting Variants
Samples
Known GenesROS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423461
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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