A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455162



Internal ID21112715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86135432..86135775hg38UCSC Ensembl
chr10:87895189..87895532hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984469
Samples
Known GenesGRID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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