A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520959



Internal ID18472554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46588384hg38UCSC Ensembl
Innerchr10:46961233..47153919hg19UCSC Ensembl
Innerchr10:46381239..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38192542
hg19192687
hg18192687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050501
Supporting Variants
Samples
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520959
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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