A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394565



Internal ID22452435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32377676..32378012hg38UCSC Ensembl
chr20:30965479..30965815hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952229
Supporting Variants
Samples
Known GenesASXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394565
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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