A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045890



Internal ID18788421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46446149..46606240hg38UCSC Ensembl
Innerchr10:46943377..47103613hg19UCSC Ensembl
Innerchr10:46363383..46523619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38160092
hg19160237
hg18160237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv763n100
Supporting Variantsnssv3709026, nssv3709027
Samples
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045890
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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