A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873479



Internal ID22648426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100651674..100652873hg38UCSC Ensembl
chr15:101191879..101193078hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470650
Samples
Known GenesASB7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873479
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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