A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1738n100



Internal ID22787825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104877181..105243289hg38UCSC Ensembl
chr13:105529532..105895640hg19UCSC Ensembl
chr13:104327533..104693641hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38366109
hg19366109
hg18366109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053363, nsv1035631
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)dgv1738n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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