A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3405n54



Internal ID22771300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111024573..111107171hg38UCSC Ensembl
chr13:111676920..111759518hg19UCSC Ensembl
chr13:110474921..110557519hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3882599
hg1982599
hg1882599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563172, nsv563173, nsv563167, nsv563168, nsv563170, nsv563174, nsv563171, nsv563166
Samples1798860569_A, 1780854058_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3405n54
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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