A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407101



Internal ID22464971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33110061..33110148hg38UCSC Ensembl
chr20:31697867..31697954hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948009
Supporting Variants
Samples
Known GenesBPIFB4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407101
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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