A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985345



Internal ID12636488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66986536..67155736hg38UCSC Ensembl
Innerchr10:68746294..68915494hg19UCSC Ensembl
Innerchr10:68416300..68585500hg18UCSC Ensembl
Innerchr10:68416300..68585500hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38169201
hg19169201
hg18169201
hg17169201
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985345
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