A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918915



Internal ID22694137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124056862..124056921hg38UCSC Ensembl
chr10:125816378..125816437hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360012
Samples
Known GenesCHST15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918915
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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