A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621317



Internal ID21813364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:15707200..15708149hg38UCSC Ensembl
chr20:15687845..15688794hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057748
Supporting Variants
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621317
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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