A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv783n100



Internal ID20152399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..46560078hg38UCSC Ensembl
chr10:46989539..47153919hg19UCSC Ensembl
chr10:46409545..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38164236
hg19164381
hg18164381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052717, nsv1041831, nsv1049662, nsv1049365
Samples
Known GenesGPRIN2, HNRNPA1P33, 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)dgv783n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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