A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880428



Internal ID22655398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15188988..15224212hg38UCSC Ensembl
chr1:15515484..15550708hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3835225
hg1935225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367305
Samples
Known GenesTMEM51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880428
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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