A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465651



Internal ID22523540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80429836..80434486hg38UCSC Ensembl
chr12:80823616..80828266hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg384651
hg194651
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465651
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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