A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052427



Internal ID18794958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:85234813..86270793hg38UCSC Ensembl
Innerchr10:86994569..88030550hg19UCSC Ensembl
Innerchr10:86984549..88020530hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381035981
hg191035982
hg181035982
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519249
Samples
Known GenesGRID1, GRID1-AS1, MIR346
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052427
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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