A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667593



Internal ID9587012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15448236..15455272hg38UCSC Ensembl
chr1:15774731..15781767hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387037
hg197037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6506394
SamplesHG01134
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667593
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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