A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936581



Internal ID22711937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36534878..36548977hg38UCSC Ensembl
chr15:36827079..36841178hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3814100
hg1914100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936581
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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