A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631609



Internal ID7018418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26572501..26574325hg38UCSC Ensembl
Innerchr13:26572533..26574294hg38UCSC Ensembl
Outerchr13:26572470..26574357hg38UCSC Ensembl
chr13:27146638..27148462hg19UCSC Ensembl
Innerchr13:27146670..27148431hg19UCSC Ensembl
Outerchr13:27146607..27148494hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381825
hg191825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14676005
SamplesNA18499
Known GenesWASF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631609
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