A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042027



Internal ID19131246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88062964..88092236hg38UCSC Ensembl
Innerchr10:89822721..89851993hg19UCSC Ensembl
Innerchr10:89812701..89841973hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3829273
hg1929273
hg1829273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508905
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042027
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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