A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445323



Internal ID21102876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85708333..85709015hg38UCSC Ensembl
chr10:87468090..87468772hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984435
Samples
Known GenesGRID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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