A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416715



Internal ID21074268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120569296..120571434hg38UCSC Ensembl
chr8:121581536..121583674hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg382139
hg192139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164248
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416715
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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