A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14837776



Internal ID3356611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89553293..89591495hg38UCSC Ensembl
Innerchr13:89553293..89591495hg38UCSC Ensembl
Outerchr13:89552793..89591995hg38UCSC Ensembl
chr13:90205547..90243749hg19UCSC Ensembl
Innerchr13:90205547..90243749hg19UCSC Ensembl
Outerchr13:90205047..90244249hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3838203
hg1938203
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633096
Supporting Variants
SamplesHG03009
Known GenesLINC00353
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14837776
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