A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv922n100



Internal ID22787009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70352092..70394751hg38UCSC Ensembl
chr10:72111848..72154507hg19UCSC Ensembl
chr10:71781854..71824513hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3842660
hg1942660
hg1842660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044989, nsv1037291
Samples
Known GenesLRRC20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv922n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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