A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660595



Internal ID9580014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15594223..15610588hg38UCSC Ensembl
chr1:15920718..15937083hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3816366
hg1916366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv17e199
Supporting Variantsessv6551508
SamplesNA19834
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660595
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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