A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039572



Internal ID20606612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26079312..26082586hg38UCSC Ensembl
chr18:23659276..23662550hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383275
hg193275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525018
Supporting Variants
Samples
Known GenesSS18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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