A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043787



Internal ID19133006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4244688..4265130hg38UCSC Ensembl
Innerchr10:4286880..4307322hg19UCSC Ensembl
Innerchr10:4276880..4297322hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3820443
hg1920443
hg1820443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv663n100
Supporting Variantsnssv3487277
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)nsv1043787
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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