A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809849



Internal ID21255187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183464341..183464406hg38UCSC Ensembl
chr4:184385494..184385559hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809849
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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