A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178076



Internal ID21316872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18776542..18776768hg38UCSC Ensembl
chr20:18757186..18757412hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954107
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178076
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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