A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511866



Internal ID18810147
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 StatusS
Merged Variantsnsv1040227
Supporting Variants
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)nssv3511866
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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