A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13982866



Internal ID3984682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132322882..132551350hg38UCSC Ensembl
chr10:134136386..134364854hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38228469
hg19228469
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624986
Supporting Variants
SamplesHG00096
Known GenesC10orf91, INPP5A, LRRC27, PWWP2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13982866
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