A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633571



Internal ID7020380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111936429..111944019hg38UCSC Ensembl
Innerchr13:111936484..111943964hg38UCSC Ensembl
Outerchr13:111936374..111944074hg38UCSC Ensembl
chr13:112590743..112598333hg19UCSC Ensembl
Innerchr13:112590798..112598278hg19UCSC Ensembl
Outerchr13:112590688..112598388hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg387591
hg197591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14899361, essv14899360
SamplesHG01366, NA19663
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633571
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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