A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043457



Internal ID19132676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47016665..47113250hg19UCSC Ensembl
Innerchr10:46436671..46533256hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1996586
hg1896586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv786n100
Supporting Variantsnssv3509975
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)nsv1043457
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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