A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15063997



Internal ID3356749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75313124..75313775hg38UCSC Ensembl
Innerchr14:75313174..75313725hg38UCSC Ensembl
Outerchr14:75313074..75313825hg38UCSC Ensembl
chr14:75779827..75780478hg19UCSC Ensembl
Innerchr14:75779877..75780428hg19UCSC Ensembl
Outerchr14:75779777..75780528hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634961
Supporting Variants
SamplesHG03009
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15063997
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