A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390318



Internal ID22448188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18268627..18273038hg38UCSC Ensembl
chr20:18249271..18253682hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384412
hg194412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390318
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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