A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3606082



Internal ID6993018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103703449..103713879hg38UCSC Ensembl
Innerchr5:103703465..103713864hg38UCSC Ensembl
Outerchr5:103703434..103713895hg38UCSC Ensembl
chr5:103039150..103049580hg19UCSC Ensembl
Innerchr5:103039166..103049565hg19UCSC Ensembl
Outerchr5:103039135..103049596hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3810431
hg1910431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12004909
SamplesHG03968
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3606082
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