A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453831



Internal ID22511706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116657274..116661131hg38UCSC Ensembl
chr12:117095079..117098936hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453831
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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