A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632676



Internal ID7019487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71452317..71461570hg38UCSC Ensembl
Innerchr13:71452317..71461570hg38UCSC Ensembl
Outerchr13:71452183..71461705hg38UCSC Ensembl
chr13:72026449..72035702hg19UCSC Ensembl
Innerchr13:72026449..72035702hg19UCSC Ensembl
Outerchr13:72026315..72035837hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg389254
hg199254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14789775
SamplesNA19712
Known GenesDACH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632676
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