A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1726n100



Internal ID22787813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89144402..89193689hg38UCSC Ensembl
chr13:89796656..89845943hg19UCSC Ensembl
chr13:88594657..88643944hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3849288
hg1949288
hg1849288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051463, nsv1043533, nsv1051653, nsv1047325, nsv1046270
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)dgv1726n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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