A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985343



Internal ID12636486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66976136..67150236hg38UCSC Ensembl
Innerchr10:68735894..68909994hg19UCSC Ensembl
Innerchr10:68405900..68580000hg18UCSC Ensembl
Innerchr10:68405900..68580000hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38174101
hg19174101
hg18174101
hg17174101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750972
Supporting Variants
SamplesSPC_15
Known GenesCTNNA3, LRRTM3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985343
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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