A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985431



Internal ID12982269
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 StatusS
Merged Variantsesv35034
Supporting Variants
SamplesNA19143
Known GenesSPRNP1, SYCE1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985431
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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