A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7342n54



Internal ID20140766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236174434..236263675hg38UCSC Ensembl
chr2:237083077..237172318hg19UCSC Ensembl
chr2:236747816..236837057hg18UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3889242
hg1989242
hg1889242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv584723, nsv584722
Samples1780862444_A
Known GenesASB18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7342n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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