A curated catalogue of human genomic structural variation




Variant Details

Variant: esv987760



Internal ID7075258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23111808..23111861hg38UCSC Ensembl
chr10:23400737..23400790hg19UCSC Ensembl
chr10:23440743..23440796hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3573397
SamplesHuRef
Known GenesMSRB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv987760
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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