A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1603n100



Internal ID19011971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18592436..18864679hg38UCSC Ensembl
chr13:19166576..19438819hg19UCSC Ensembl
chr13:18064576..18336819hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38272244
hg19272244
hg18272244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035960, nsv1048594, nsv1044688
Samples
Known GenesANKRD20A9P, LINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1603n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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