A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv28n97



Internal ID22815425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6933714..6947777hg38UCSC Ensembl
chr10:6975676..6989739hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3814064
hg1914064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154548, nsv1154549
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv28n97
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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