A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052717



Internal ID18795248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46995683..47121369hg19UCSC Ensembl
Innerchr10:46415689..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19125687
hg18125687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv783n100
Supporting Variantsnssv3515155
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)nsv1052717
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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