A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002005



Internal ID6714139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13211837..13220494hg38UCSC Ensembl
Outerchr10:13253837..13262494hg19UCSC Ensembl
Outerchr10:13293843..13302500hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg388658
hg198658
hg188658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565027
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002005
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