A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659605



Internal ID9579024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99661965..99688452hg38UCSC Ensembl
Innerchr10:101421722..101448209hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3826488
hg1926488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5578816
SamplesNA19238
Known GenesENTPD7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659605
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer