A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690092



Internal ID21211944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47923118..47923192hg38UCSC Ensembl
chr4:47925135..47925209hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690092
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.5625


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