A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508697



Internal ID18460292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46994321..47121369hg19UCSC Ensembl
Innerchr10:46414327..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19127049
hg18127049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041831
Supporting Variants
Samples
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508697
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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