A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059961



Internal ID20627001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28571798..28599590hg38UCSC Ensembl
chr1:28898310..28926102hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3827793
hg1927793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322009
Supporting Variants
Samples
Known GenesRAB42, SNHG12, SNORA16A, SNORA44, SNORA61, SNORD99, TRNAU1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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