A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513926



Internal ID18465521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46481226..46631445hg38UCSC Ensembl
Innerchr10:46918172..47068231hg19UCSC Ensembl
Innerchr10:46338178..46488237hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38150220
hg19150060
hg18150060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044141
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)nssv3513926
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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