A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14671213



Internal ID4673029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24459706..24465612hg38UCSC Ensembl
Innerchr13:24459737..24465582hg38UCSC Ensembl
Outerchr13:24459676..24465643hg38UCSC Ensembl
chr13:25033844..25039750hg19UCSC Ensembl
Innerchr13:25033875..25039720hg19UCSC Ensembl
Outerchr13:25033814..25039781hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg385907
hg195907
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631558
Supporting Variants
SamplesHG03693
Known GenesPARP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14671213
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