A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705233



Internal ID21227039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77725415..77725415hg38UCSC Ensembl
chr7:77354732..77354732hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2815639
Supporting Variants
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705233
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.578125


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