A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047766



Internal ID19136985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65563025..65583684hg38UCSC Ensembl
Innerchr10:67322783..67343442hg19UCSC Ensembl
Innerchr10:66992789..67013448hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3820660
hg1920660
hg1820660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv891n100
Supporting Variantsnssv3514271
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)nsv1047766
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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