A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828254



Internal ID22603189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15714652..15739601hg38UCSC Ensembl
chr1:16041147..16066096hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3824950
hg1924950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466365
Samples
Known GenesPLEKHM2, SLC25A34
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828254
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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