A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042880



Internal ID20609920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45488189..45488999hg38UCSC Ensembl
chr18:43068154..43068964hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38811
hg19811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519214
Supporting Variants
Samples
Known GenesSLC14A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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