A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179332



Internal ID21318128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4227652..4227704hg38UCSC Ensembl
chr20:4208299..4208351hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3955091
Supporting Variants
SamplesHG002
Known GenesADRA1D
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179332
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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