A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059719



Internal ID20626759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28216201..28219500hg38UCSC Ensembl
chr1:28542712..28546011hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322008
Supporting Variants
Samples
Known GenesDNAJC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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