A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1654n100



Internal ID22787741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53354060..53382334hg38UCSC Ensembl
chr13:53928195..53956469hg19UCSC Ensembl
chr13:52826196..52854470hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3828275
hg1928275
hg1828275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051184, nsv1040236
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)dgv1654n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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