A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633573



Internal ID7020382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112174376..112183597hg38UCSC Ensembl
Innerchr13:112174876..112183097hg38UCSC Ensembl
Outerchr13:112173376..112184597hg38UCSC Ensembl
chr13:112828690..112837911hg19UCSC Ensembl
Innerchr13:112829190..112837411hg19UCSC Ensembl
Outerchr13:112827690..112838911hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg389222
hg199222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv375e214
Supporting Variantsessv14899363
SamplesHG02057
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633573
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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