A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633392



Internal ID7020201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103059986..103070188hg38UCSC Ensembl
chr13:103712336..103722538hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3810203
hg1910203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv364e214
Supporting Variantsessv14881031, essv14881029, essv14881030
SamplesHG02012, HG01398, HG01183
Known GenesSLC10A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633392
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer