A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1684n100



Internal ID22787771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63453454..63499844hg38UCSC Ensembl
chr13:64027587..64073977hg19UCSC Ensembl
chr13:62925588..62971978hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3846391
hg1946391
hg1846391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041530, nsv1038853
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)dgv1684n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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