A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565028



Internal ID7036128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98055494..98062593hg38UCSC Ensembl
Outerchr10:99815251..99822350hg19UCSC Ensembl
Outerchr10:99805241..99812340hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg387100
hg197100
hg187100
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1011312
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565028
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