A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060963



Internal ID20628003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33218351..33223149hg38UCSC Ensembl
chr1:33683952..33688750hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384799
hg194799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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