A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050796



Internal ID18793327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46918172..47058976hg19UCSC Ensembl
Innerchr10:46338178..46478982hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19140805
hg18140805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv750n100
Supporting Variantsnssv3517321
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)nsv1050796
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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