A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9709n54



Internal ID22777604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28806149..28902719hg38UCSC Ensembl
chr5:28806256..28902826hg19UCSC Ensembl
chr5:28842013..28938583hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3896571
hg1996571
hg1896571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597729, nsv597738
SamplesNINDS_142, NINDS_189
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9709n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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