A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3411n100



Internal ID22789498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78622921..78681382hg38UCSC Ensembl
chr18:76382921..76441382hg19UCSC Ensembl
chr18:74483909..74542370hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3858462
hg1958462
hg1858462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056784, nsv1056545
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3411n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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