A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038734



Internal ID20605774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11825628..11829907hg38UCSC Ensembl
chr18:11825627..11829906hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384280
hg194280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535394
Supporting Variants
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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