A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3417n100



Internal ID20155033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80197495..80257174hg38UCSC Ensembl
chr18:77955378..78015057hg19UCSC Ensembl
chr18:76056369..76116029hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3859680
hg1959680
hg1859661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057565, nsv1060370
Samples
Known GenesPARD6G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3417n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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