A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415910



Internal ID21073463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99057532..99581086hg38UCSC Ensembl
chr8:100069760..100593314hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38523555
hg19523555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173596
Samples
Known GenesMIR599, MIR875, VPS13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415910
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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