A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13864483



Internal ID3866299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76202051..76206290hg38UCSC Ensembl
chr10:77961809..77966048hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg384240
hg194240
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623863
Supporting Variants
SamplesHG03985
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13864483
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