A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883992



Internal ID22658974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90821373..90823572hg38UCSC Ensembl
chr15:91364603..91366802hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883992
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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