A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670722



Internal ID9590141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30962519..30964103hg38UCSC Ensembl
chr15:31254722..31256306hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381585
hg191585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6003973, essv6519218, essv6422366
SamplesHG00369, HG00270, HG00156
Known GenesMTMR10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670722
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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