A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5554n54



Internal ID20138978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36184860..36195497hg38UCSC Ensembl
chr17:34600294..34610939hg19UCSC Ensembl
chr17:31624407..31635052hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810638
hg1910646
hg1810646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574833, nsv574842, nsv574843
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5554n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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