A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1740n100



Internal ID22787827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107456259..107559672hg38UCSC Ensembl
chr13:108108607..108212020hg19UCSC Ensembl
chr13:106906608..107010021hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38103414
hg19103414
hg18103414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054176, nsv1039280
Samples
Known GenesFAM155A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1740n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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