A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv992n54



Internal ID22768887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20533677..20565668hg38UCSC Ensembl
chr10:20822606..20854597hg19UCSC Ensembl
chr10:20862612..20894603hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3831992
hg1931992
hg1831992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550160, nsv550159, nsv550158
Samples1780854455_A
Known GenesMIR4675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv992n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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