A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464241



Internal ID22522127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46943776..46945357hg38UCSC Ensembl
chr12:47337559..47339140hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464241
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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