A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636443



Internal ID7023237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50501237..50504753hg38UCSC Ensembl
Innerchr15:50501244..50504747hg38UCSC Ensembl
Outerchr15:50501231..50504760hg38UCSC Ensembl
chr15:50793434..50796950hg19UCSC Ensembl
Innerchr15:50793441..50796944hg19UCSC Ensembl
Outerchr15:50793428..50796957hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383517
hg193517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15246899
SamplesHG01797
Known GenesUSP50
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636443
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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