A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519742



Internal ID18471337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46536457..46631445hg38UCSC Ensembl
Innerchr10:46918172..47013160hg19UCSC Ensembl
Innerchr10:46338178..46433166hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3894989
hg1994989
hg1894989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047710
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)nssv3519742
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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