A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870027



Internal ID22644962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89746400..89751050hg38UCSC Ensembl
chr15:90289631..90294281hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384651
hg194651
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474363
Samples
Known GenesMESP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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