A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6504805



Internal ID9482208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21222370..21227289hg38UCSC Ensembl
chr14:21690529..21695448hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg384920
hg194920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656744
Supporting Variants
SamplesNA19385
Known GenesHNRNPC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6504805
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer