A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697077



Internal ID21218926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2378444..2378507hg38UCSC Ensembl
chr7:2418079..2418142hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816532
Supporting Variants
Samples
Known GenesEIF3B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697077
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.609375


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