A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11937n54



Internal ID22779832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8236884..8287918hg38UCSC Ensembl
chr8:8094406..8145440hg19UCSC Ensembl
chr8:8131816..8182850hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3851035
hg1951035
hg1851035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610150, nsv610148
Samples1780862274_A, NINDS_37, 1782681555_A, NINDS_152, HGDP00512, HGDP01362, HGDP01077, 1782681176_A
Known GenesFAM86B3P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11937n54
Frequency
Sample Size17421
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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