A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505148



Internal ID18803429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66515998..66737409hg38UCSC Ensembl
Innerchr10:68275756..68497167hg19UCSC Ensembl
Innerchr10:67945762..68167173hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38221412
hg19221412
hg18221412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037600
Supporting Variants
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505148
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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