A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050696



Internal ID18793227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46545925..46588384hg38UCSC Ensembl
Innerchr10:46961233..47003692hg19UCSC Ensembl
Innerchr10:46381239..46423698hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3842460
hg1942460
hg1842460
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517205
Samples
Known GenesGPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050696
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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