A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13982867



Internal ID3984683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132338306..132366249hg38UCSC Ensembl
chr10:134151810..134179753hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3827944
hg1927944
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624988
Supporting Variants
SamplesHG00096
Known GenesLRRC27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13982867
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