A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv771n100



Internal ID20152387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46529453..46588384hg38UCSC Ensembl
chr10:46961233..47020164hg19UCSC Ensembl
chr10:46381239..46440170hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3858932
hg1958932
hg1858932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035226, nsv1043525
Samples
Known GenesGPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv771n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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