A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416434



Internal ID21073987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10241151..10322884hg38UCSC Ensembl
chr8:10098661..10180394hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3881734
hg1981734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162492
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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