A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403264



Internal ID22461134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11649053..11649107hg38UCSC Ensembl
chr20:11629701..11629755hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403264
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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