A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865653



Internal ID22640588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:29179436..29182150hg38UCSC Ensembl
chr15:29471639..29474353hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382715
hg192715
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471110
Samples
Known GenesFAM189A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865653
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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