A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802535



Internal ID21247873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33093541..33093643hg38UCSC Ensembl
chr20:31681347..31681449hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691241
Samples
Known GenesBPIFB4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802535
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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