A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv941n100



Internal ID20152557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79884324..80099035hg38UCSC Ensembl
chr10:81644080..81858791hg19UCSC Ensembl
chr10:81634060..81848771hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38214712
hg19214712
hg18214712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037922, nsv1051203
Samples
Known GenesLOC100288974, MBL1P, SFTPD, TMEM254, TMEM254-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv941n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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