A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1733n100



Internal ID22787820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102046039..102107847hg38UCSC Ensembl
chr13:102698389..102760197hg19UCSC Ensembl
chr13:101496390..101558198hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3861809
hg1961809
hg1861809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045176, nsv1039315
Samples
Known GenesFGF14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1733n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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