A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429975



Internal ID21087528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13214712..13223190hg38UCSC Ensembl
chr8:13072221..13080699hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388479
hg198479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165684
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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