A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664564



Internal ID9930669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23222574..23224019hg38UCSC Ensembl
chr7:23262193..23263638hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6373192, essv5637799, essv6471084, essv6257094
SamplesNA19373, NA19313, NA19625, HG01108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664564
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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