A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288033



Internal ID20497251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51732651..51732651hg38UCSC Ensembl
chr20:50349190..50349190hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759079
Supporting Variants
Samples
Known GenesATP9A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288033
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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