A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103712



Internal ID4905015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97419131..97423595hg38UCSC Ensembl
Innerchr14:97419131..97423595hg38UCSC Ensembl
Outerchr14:97419104..97423763hg38UCSC Ensembl
chr14:97885468..97889932hg19UCSC Ensembl
Innerchr14:97885468..97889932hg19UCSC Ensembl
Outerchr14:97885441..97890100hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384465
hg194465
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635442
Supporting Variants
SamplesNA12717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103712
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