A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7088n54



Internal ID20140512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134101185..134137859hg38UCSC Ensembl
chr2:134858756..134895430hg19UCSC Ensembl
chr2:134575226..134611900hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3836675
hg1936675
hg1836675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv583169, nsv583170
Samples
Known GenesMIR3679
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7088n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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