A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451565



Internal ID22509437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92679768..92686744hg38UCSC Ensembl
chr12:93073544..93080520hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg386977
hg196977
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850564
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451565
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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