A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367154



Internal ID22592823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103230114..103230223hg38UCSC Ensembl
chr12:103623892..103624001hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367154
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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