A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1406n54



Internal ID22769301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121672674..121702140hg38UCSC Ensembl
chr10:123432188..123461654hg19UCSC Ensembl
chr10:123422178..123451644hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3829467
hg1929467
hg1829467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552235, nsv552234, nsv552240, nsv552239, nsv552241, nsv552242
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1406n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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