A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1718n100



Internal ID22787805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83525987..83581865hg38UCSC Ensembl
chr13:84100122..84156000hg19UCSC Ensembl
chr13:82998123..83054001hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3855879
hg1955879
hg1855879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038892, nsv1051050, nsv1042857, nsv1039944, nsv1043297, nsv1039670, nsv1045865, nsv1053461
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)dgv1718n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss55
Observed Complex0
Frequencyn/a


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