A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv767n100



Internal ID20152383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46332711..46595134hg38UCSC Ensembl
chr10:46954483..47249575hg19UCSC Ensembl
chr10:46374489..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38262424
hg19295093
hg18295093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036977, nsv1052336, nsv1049405, nsv1045027, nsv1049147, nsv1047560, nsv1049239
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, GPRIN2, HNRNPA1P33, 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)dgv767n100
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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