A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv768n100



Internal ID20152384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46553382..46592975hg38UCSC Ensembl
chr10:46956642..46996235hg19UCSC Ensembl
chr10:46376648..46416241hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3839594
hg1939594
hg1839594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054377, nsv1046276
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)dgv768n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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