A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674602



Internal ID9940707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27629792..27635149hg38UCSC Ensembl
chr9:27629790..27635147hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg385358
hg195358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1332e199
Supporting Variantsessv6027651
SamplesHG00120
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674602
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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