A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13693603



Internal ID21215455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25450819..25450879hg38UCSC Ensembl
chr12:25603753..25603813hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13693603
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.40625


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