A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037600



Internal ID19126819
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 StatusM
Merged Variantsdgv902n100
Supporting Variantsnssv3505148
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)nsv1037600
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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