A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417003



Internal ID21074556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52212193..52219357hg38UCSC Ensembl
chr8:53124753..53131917hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg387165
hg197165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168295
Samples
Known GenesST18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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