A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456547



Internal ID22514425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40139397..40145485hg38UCSC Ensembl
chr12:40533199..40539287hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg386089
hg196089
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456547
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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