A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923068



Internal ID22698294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17021185..17040992hg38UCSC Ensembl
chr10:17063184..17082991hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3819808
hg1919808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364662
Samples
Known GenesCUBN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923068
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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