A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704076



Internal ID21225882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30246699..30246775hg38UCSC Ensembl
chr8:30104215..30104291hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818496
Supporting Variants
Samples
Known GenesMIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704076
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.553571


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