A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040227



Internal ID19129446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47003692..47094632hg19UCSC Ensembl
Innerchr10:46423698..46514638hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1990941
hg1890941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv776n100
Supporting Variantsnssv3511866
Samples
Known GenesLOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040227
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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