A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv968n100



Internal ID22787055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105340152..105557234hg38UCSC Ensembl
chr10:107099910..107316992hg19UCSC Ensembl
chr10:107089900..107306982hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38217083
hg19217083
hg18217083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052152, nsv1055076, nsv1047197, nsv1053012, nsv1037762, nsv1037911, nsv1050152, nsv1047422, nsv1049260, nsv1037086, nsv1048698, nsv1043393, nsv1051395, nsv1048837
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv968n100
Frequency
Sample Size11257
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


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