A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809844



Internal ID21255182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182124897..182124957hg38UCSC Ensembl
chr4:183046050..183046110hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13710020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809844
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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