A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808255



Internal ID21253593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197030147..197030314hg38UCSC Ensembl
chr3:196757018..196757185hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808255
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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