A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678026



Internal ID21199883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:220902..220902hg38UCSC Ensembl
chr17:70693..70693hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797095
Supporting Variants
Samples
Known GenesRPH3AL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678026
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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