A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv361e199



Internal ID22758134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71452316..71461591hg38UCSC Ensembl
chr13:72026448..72035723hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg389276
hg199276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668619, esv2662734
SamplesNA19712
Known GenesDACH1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv361e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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