A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9934n54



Internal ID22777829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90954083..91011335hg38UCSC Ensembl
chr5:90249900..90307152hg19UCSC Ensembl
chr5:90285656..90342908hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3857253
hg1957253
hg1857253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598929, nsv598930, nsv598928, nsv598931
Samples1780854061_A
Known GenesGPR98
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9934n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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