A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15114224



Internal ID1944737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103200275..103247803hg38UCSC Ensembl
Innerchr14:103200775..103247303hg38UCSC Ensembl
Outerchr14:103199275..103248803hg38UCSC Ensembl
chr14:103666612..103714140hg19UCSC Ensembl
Innerchr14:103667112..103713640hg19UCSC Ensembl
Outerchr14:103665612..103715140hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3847529
hg1947529
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635580
Supporting Variants
SamplesHG01806
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15114224
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