A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669536



Internal ID9935641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124064908..124076790hg38UCSC Ensembl
chr7:123704962..123716844hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3811883
hg1911883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6034186
SamplesNA19472
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669536
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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