A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985344



Internal ID12636487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66986527..67155754hg38UCSC Ensembl
Innerchr10:68746285..68915512hg19UCSC Ensembl
Innerchr10:68416291..68585518hg18UCSC Ensembl
Innerchr10:68416291..68585518hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38169228
hg19169228
hg18169228
hg17169228
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)essv6985344
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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