A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1411n54



Internal ID22769306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122584746..122593059hg38UCSC Ensembl
chr10:124344262..124352575hg19UCSC Ensembl
chr10:124334252..124342565hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg388314
hg198314
hg188314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552270, nsv552258, nsv552268, nsv552267, nsv552259, nsv552260, nsv552269, nsv552261, nsv552257
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1411n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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