A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061926



Internal ID20628966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58841692..58845409hg38UCSC Ensembl
chr1:59307364..59311081hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg383718
hg193718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318559
Supporting Variants
Samples
Known GenesLINC01135
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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