A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421187



Internal ID21078740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13147842..13159955hg38UCSC Ensembl
chr8:13005351..13017464hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3812114
hg1912114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165624
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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