A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656840



Internal ID9922945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:3785450..3800634hg38UCSC Ensembl
OuterchrX:3785293..3800787hg38UCSC Ensembl
InnerchrX:3703491..3718675hg19UCSC Ensembl
OuterchrX:3703334..3718828hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3815495
hg1915495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5792880
SamplesNA18501
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656840
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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