A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400693



Internal ID22458563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35322485..35322588hg38UCSC Ensembl
chr20:33910288..33910391hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955058
Supporting Variants
Samples
Known GenesUQCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400693
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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