A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708182



Internal ID21229972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22418526..22425165hg38UCSC Ensembl
chr12:22571460..22578099hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg386640
hg196640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708182
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.96875


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