A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511486



Internal ID18463081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46918172..47058961hg19UCSC Ensembl
Innerchr10:46338178..46478967hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19140790
hg18140790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044979
Supporting Variants
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)nssv3511486
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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