A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431618



Internal ID21089171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120475001..120476700hg38UCSC Ensembl
chr8:121487241..121488940hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164243
Samples
Known GenesMTBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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