A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515675



Internal ID20889036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26343244..26351476hg38UCSC Ensembl
chr18:23923208..23931440hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg388233
hg198233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039580
Samples
Known GenesTAF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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