A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15059527



Internal ID2772204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73561433..73573896hg38UCSC Ensembl
chr14:74028137..74040600hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3812464
hg1912464
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634914
Supporting Variants
SamplesHG02445
Known GenesACOT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15059527
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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