A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv750n100



Internal ID19011118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46469221..46631445hg38UCSC Ensembl
chr10:46918172..47080230hg19UCSC Ensembl
chr10:46338178..46500236hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38162225
hg19162059
hg18162059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050796, nsv1044979, nsv1037637
Samples
Known GenesFAM35BP, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv750n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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