A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050898



Internal ID18793429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46411170..46462388hg38UCSC Ensembl
Innerchr10:47087031..47138582hg19UCSC Ensembl
Innerchr10:46507037..46558588hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3851219
hg1951552
hg1851552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv821n100
Supporting Variantsnssv3517431
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)nsv1050898
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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