A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2803096



Internal ID21248434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32176437..32176788hg38UCSC Ensembl
chr20:30764240..30764591hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2803096
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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