A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046878



Internal ID18789409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46446149..46489856hg38UCSC Ensembl
Innerchr10:47055642..47103613hg19UCSC Ensembl
Innerchr10:46475648..46523619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3843708
hg1947972
hg1847972
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705841, nssv3509513
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)nsv1046878
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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