A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886629



Internal ID22661618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90652492..90661759hg38UCSC Ensembl
chr15:91195723..91204990hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg389268
hg199268
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886629
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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