A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050503



Internal ID18793034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46449893..46489856hg38UCSC Ensembl
Innerchr10:47058780..47099869hg19UCSC Ensembl
Innerchr10:46478786..46519875hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3839964
hg1941090
hg1841090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv811n100
Supporting Variantsnssv3520960
Samples
Known GenesLINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050503
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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