A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404997



Internal ID22462867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44864953..44865629hg38UCSC Ensembl
chr20:43493594..43494270hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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