A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14699263



Internal ID669165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38545827..38606832hg38UCSC Ensembl
Innerchr13:38545836..38606823hg38UCSC Ensembl
Outerchr13:38545818..38606841hg38UCSC Ensembl
chr13:39119964..39180969hg19UCSC Ensembl
Innerchr13:39119973..39180960hg19UCSC Ensembl
Outerchr13:39119955..39180978hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3861006
hg1961006
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631822
Supporting Variants
SamplesHG00311
Known GenesLINC00366
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14699263
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