A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417482



Internal ID21075035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50403201..50405800hg38UCSC Ensembl
chr8:51315761..51318360hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167535
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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