A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11066222



Internal ID2914600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88155868..88168209hg38UCSC Ensembl
chr3:88205018..88217359hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3812342
hg1912342
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596915
Supporting Variants
SamplesHG02582
Known GenesC3orf38
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11066222
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