A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15217021



Internal ID5218837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36911173..36955710hg38UCSC Ensembl
chr15:37203374..37247911hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3844538
hg1944538
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636165
Supporting Variants
SamplesHG00365
Known GenesMEIS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15217021
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