A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687392



Internal ID21209256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:611358..611425hg38UCSC Ensembl
chr4:605147..605214hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687392
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.171875


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