A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429791



Internal ID21087344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120601287..120601936hg38UCSC Ensembl
chr8:121613527..121614176hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164251
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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