A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360365



Internal ID22586034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115579515..115579591hg38UCSC Ensembl
chr12:116017320..116017396hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360365
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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