A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707726



Internal ID21229519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155733468..155733468hg38UCSC Ensembl
chr7:155526162..155526162hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2815980
Supporting Variants
Samples
Known GenesRBM33
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707726
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.328125


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