A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931279



Internal ID22706561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81125060..81134679hg38UCSC Ensembl
chr15:81417401..81427020hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg389620
hg199620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378873
Samples
Known GenesC15orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931279
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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