A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849832



Internal ID22624767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51278627..51283576hg38UCSC Ensembl
chr15:51570824..51575773hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg384950
hg194950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472828
Samples
Known GenesCYP19A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849832
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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