A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656494



Internal ID9922599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119578344..119593805hg38UCSC Ensembl
chr7:119218398..119233859hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3815462
hg1915462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6302541, essv6022296
SamplesNA19908, NA19463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656494
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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