A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465807



Internal ID22523696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46374569..46375867hg38UCSC Ensembl
chr12:46768352..46769650hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg381299
hg191299
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465807
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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