A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039377



Internal ID18781908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46440224..46588384hg38UCSC Ensembl
Innerchr10:46961233..47109535hg19UCSC Ensembl
Innerchr10:46381239..46529541hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38148161
hg19148303
hg18148303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv763n100
Supporting Variantsnssv3505861
Samples
Known GenesGPRIN2, 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)nsv1039377
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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