A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv822n100



Internal ID20152438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..46446149hg38UCSC Ensembl
chr10:47103613..47153919hg19UCSC Ensembl
chr10:46523619..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3850307
hg1950307
hg1850307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046010, nsv1049183, nsv1040642
Samples
Known GenesHNRNPA1P33, LINC00842
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv822n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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