A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037295



Internal ID19126514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66988698..67015760hg38UCSC Ensembl
Innerchr10:68748456..68775518hg19UCSC Ensembl
Innerchr10:68418462..68445524hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3827063
hg1927063
hg1827063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706103
Samples
Known GenesCTNNA3, LRRTM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037295
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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