A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054508



Internal ID18797039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34729183..35050396hg38UCSC Ensembl
Innerchr10:35018111..35339324hg19UCSC Ensembl
Innerchr10:35058117..35379330hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38321214
hg19321214
hg18321214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv703n100
Supporting Variantsnssv3522197
Samples
Known GenesCUL2, PARD3, PARD3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054508
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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