A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139550



Internal ID20706590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1248224..1424459hg38UCSC Ensembl
chr6:1248459..1424694hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38176236
hg19176236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400271
Supporting Variants
Samples
Known GenesFOXF2, FOXQ1, MIR6720
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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