A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037550



Internal ID19126769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108065569..108125649hg38UCSC Ensembl
Innerchr10:109825327..109885407hg19UCSC Ensembl
Innerchr10:109815317..109875397hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3860081
hg1960081
hg1860081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv972n100
Supporting Variantsnssv3505090
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)nsv1037550
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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