A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433033



Internal ID21090586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120565089..120570604hg38UCSC Ensembl
chr8:121577329..121582844hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg385516
hg195516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164247
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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