A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449832



Internal ID22507702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55589134..55593498hg38UCSC Ensembl
chr12:55982918..55987282hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg384365
hg194365
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449832
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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