A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855013



Internal ID22629948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75435411..75441675hg38UCSC Ensembl
chr15:75727752..75734016hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg386265
hg196265
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472312
Samples
Known GenesSIN3A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855013
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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