A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35157



Internal ID12991193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133557601..133609001hg38UCSC Ensembl
Innerchr10:135371105..135422505hg19UCSC Ensembl
Innerchr10:135221095..135272495hg18UCSC Ensembl
Innerchr10:135259986..135311386hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3851401
hg1951401
hg1851401
hg1751401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6980835, essv6980834
SamplesNA19132
Known GenesSPRNP1, SYCE1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35157
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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