A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707233



Internal ID21229034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69094125..69094448hg38UCSC Ensembl
chr4:69959843..69960166hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707233
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.734375


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