A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1737n100



Internal ID22787824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104763258..104797192hg38UCSC Ensembl
chr13:105415609..105449543hg19UCSC Ensembl
chr13:104213610..104247544hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3833935
hg1933935
hg1833935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051518, nsv1035344, nsv1049107
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)dgv1737n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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