A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408085



Internal ID22465955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35581444..35585174hg38UCSC Ensembl
chr20:34169366..34173096hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383731
hg193731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408085
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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