A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1405n54



Internal ID22769300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121009763..121028249hg38UCSC Ensembl
chr10:122769276..122787762hg19UCSC Ensembl
chr10:122759266..122777752hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3818487
hg1918487
hg1818487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552226, nsv552225, nsv552231, nsv552230, nsv552229, nsv552227, nsv552228
SamplesNINDS_142, HGDP01028, HGDP01408, HGDP01085, HGDP01405, HGDP00620
Known GenesMIR5694
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1405n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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