A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631596



Internal ID7018405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26240289..26241946hg38UCSC Ensembl
Innerchr13:26240348..26241887hg38UCSC Ensembl
Outerchr13:26240230..26242005hg38UCSC Ensembl
chr13:26814426..26816083hg19UCSC Ensembl
Innerchr13:26814485..26816024hg19UCSC Ensembl
Outerchr13:26814367..26816142hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381658
hg191658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14673306, essv14673304, essv14673305
SamplesNA21142, NA20851, NA21093
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631596
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