A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv342e199



Internal ID22758115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31369518..31371888hg38UCSC Ensembl
chr13:31943655..31946025hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382371
hg192371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677183, esv2671765
SamplesHG00537
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv342e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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