A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450732



Internal ID21108285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117306401..117308300hg38UCSC Ensembl
chr10:119065912..119067811hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978311
Samples
Known GenesPDZD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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