A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632367



Internal ID7019176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62233111..62315799hg38UCSC Ensembl
Innerchr13:62233127..62315783hg38UCSC Ensembl
Outerchr13:62233095..62315815hg38UCSC Ensembl
chr13:62807244..62889932hg19UCSC Ensembl
Innerchr13:62807260..62889916hg19UCSC Ensembl
Outerchr13:62807228..62889948hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3882689
hg1982689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14768534
SamplesNA20505
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632367
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