A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866624



Internal ID22641559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43996422..43998842hg38UCSC Ensembl
chr15:44288620..44291040hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471641
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866624
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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