A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678480



Internal ID21200344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47976145..47976234hg38UCSC Ensembl
chr4:47978162..47978251hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810657
Supporting Variants
Samples
Known GenesCNGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678480
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.53125


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