A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058355



Internal ID20625395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225464429..225489702hg38UCSC Ensembl
chr1:225652131..225677404hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3825274
hg1925274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321273
Supporting Variants
Samples
Known GenesENAH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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