A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7308n100



Internal ID20158924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123883276..124008232hg38UCSC Ensembl
chr8:124895516..125020472hg19UCSC Ensembl
chr8:124964697..125089653hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38124957
hg19124957
hg18124957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033617, nsv1035035
Samples
Known GenesFER1L6, FER1L6-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7308n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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