A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049466



Internal ID18791997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46918172..47059809hg19UCSC Ensembl
Innerchr10:46338178..46479815hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19141638
hg18141638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv751n100
Supporting Variantsnssv3522075, nssv3513026, nssv3517646, nssv3507552
Samples
Known GenesFAM35BP, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049466
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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