A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047259



Internal ID18789790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46487142hg38UCSC Ensembl
Innerchr10:47062299..47142310hg19UCSC Ensembl
Innerchr10:46482305..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3879705
hg1980012
hg1880012
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv801n100
Supporting Variantsnssv3517032
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)nsv1047259
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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