A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395912



Internal ID22453782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31613697..31748884hg38UCSC Ensembl
chr20:30201500..30336687hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38135188
hg19135188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962657
Supporting Variants
Samples
Known GenesBCL2L1, COX4I2, TPX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395912
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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