A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939239



Internal ID22714629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68274646..68274699hg38UCSC Ensembl
chr15:68566984..68567037hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939239
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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