A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035576



Internal ID19124795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67586596..67688531hg38UCSC Ensembl
Innerchr10:69346354..69448289hg19UCSC Ensembl
Innerchr10:69016360..69118295hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38101936
hg19101936
hg18101936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv917n100
Supporting Variantsnssv3503923
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)nsv1035576
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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