A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752276



Internal ID21390056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53468710..53469773hg38UCSC Ensembl
chr20:52085249..52086312hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433283
Supporting Variants
SamplesNB10
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752276
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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