A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933612



Internal ID22708926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84699704..84700507hg38UCSC Ensembl
chr15:85242935..85243738hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380092
Samples
Known GenesSEC11A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933612
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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