A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv985n100



Internal ID22787072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121673138..121703845hg38UCSC Ensembl
chr10:123432652..123463359hg19UCSC Ensembl
chr10:123422642..123453349hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3830708
hg1930708
hg1830708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053862, nsv1042995, nsv1044653, nsv1047566, nsv1045213, nsv1053561, nsv1038696, nsv1050025, nsv1040611, nsv1048568
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)dgv985n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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