A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042507



Internal ID20609547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55614601..55615900hg38UCSC Ensembl
chr18:53281832..53283131hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533467
Supporting Variants
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042507
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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