A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14951580



Internal ID6551934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28595512..28605555hg38UCSC Ensembl
Innerchr14:28595512..28605555hg38UCSC Ensembl
Outerchr14:28595348..28605748hg38UCSC Ensembl
chr14:29064718..29074761hg19UCSC Ensembl
Innerchr14:29064718..29074761hg19UCSC Ensembl
Outerchr14:29064554..29074954hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3810044
hg1910044
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633916
Supporting Variants
SamplesNA20753
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14951580
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