A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450650



Internal ID22508522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39745113..39748760hg38UCSC Ensembl
chr12:40138915..40142562hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg383648
hg193648
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450650
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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