A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv29e196



Internal ID22757699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111181670..111518018hg38UCSC Ensembl
chr7:110821726..111158074hg19UCSC Ensembl
chr7:110608962..110945310hg18UCSC Ensembl
chr7:110415677..110752025hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38336349
hg19336349
hg18336349
hg17336349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2422443, esv2422497
SamplesND01675, ND04534
Known GenesIMMP2L
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)dgv29e196
Frequency
Sample Size181
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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