A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054913



Internal ID19144132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34214745..34241837hg38UCSC Ensembl
Innerchr10:34503673..34530765hg19UCSC Ensembl
Innerchr10:34543679..34570771hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3827093
hg1927093
hg1827093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707749
Samples
Known GenesPARD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054913
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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