A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867007



Internal ID22641942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83636491..83642629hg38UCSC Ensembl
chr15:84305243..84311381hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386139
hg196139
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867007
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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