A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059948



Internal ID20626988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28483680..28484847hg38UCSC Ensembl
chr1:28810192..28811359hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381168
hg191168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315763
Supporting Variants
Samples
Known GenesPHACTR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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