A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059963



Internal ID20627003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28578023..28580113hg38UCSC Ensembl
chr1:28904535..28906625hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382091
hg192091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321067
Supporting Variants
Samples
Known GenesSNHG12, SNORA61, SNORD99, TRNAU1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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