A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1657n100



Internal ID22787744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:55294078..55404093hg38UCSC Ensembl
chr13:55868213..55978228hg19UCSC Ensembl
chr13:54766214..54876229hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38110016
hg19110016
hg18110016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042462, nsv1037233
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)dgv1657n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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