A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043350



Internal ID18785881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46399305..46489856hg38UCSC Ensembl
Innerchr10:47058780..47150458hg19UCSC Ensembl
Innerchr10:46478786..46570464hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3890552
hg1991679
hg1891679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv803n100
Supporting Variantsnssv3509854
Samples
Known GenesHNRNPA1P33, LINC00842, 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)nsv1043350
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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