A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036534



Internal ID19125753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66975498..67162077hg38UCSC Ensembl
Innerchr10:68735256..68921835hg19UCSC Ensembl
Innerchr10:68405262..68591841hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38186580
hg19186580
hg18186580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv916n100
Supporting Variantsnssv3706101, nssv3509858, nssv3706102, nssv3516807
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)nsv1036534
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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