A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038958



Internal ID20605998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21534598..21535500hg38UCSC Ensembl
chr18:19114559..19115461hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530960
Supporting Variants
Samples
Known GenesESCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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