A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053951



Internal ID19143170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52760817..52775673hg38UCSC Ensembl
Innerchr10:54520577..54535433hg19UCSC Ensembl
Innerchr10:54190583..54205439hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3814857
hg1914857
hg1814857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv855n100
Supporting Variantsnssv3521149
Samples
Known GenesMBL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053951
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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