A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433982



Internal ID21091535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127952973..127962156hg38UCSC Ensembl
chr8:128965219..128974402hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg389184
hg199184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163823
Samples
Known GenesMIR1205, PVT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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