A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660472



Internal ID9926577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32503490..32508355hg38UCSC Ensembl
chr1:32969091..32973956hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384866
hg194866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6218541
SamplesNA18606
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660472
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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