A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931273



Internal ID22706555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41311822..41312231hg38UCSC Ensembl
chr15:41604020..41604429hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371652
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931273
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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