A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450819



Internal ID21108372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85918250..85924317hg38UCSC Ensembl
chr10:87678007..87684074hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg386068
hg196068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984456
Samples
Known GenesGRID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450819
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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