A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453563



Internal ID22511437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:82312638..82314328hg38UCSC Ensembl
chr12:82706417..82708107hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453563
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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