A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863779



Internal ID22638714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26737295..26738564hg38UCSC Ensembl
chr15:26982442..26983711hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381270
hg191270
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471057
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863779
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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