A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5792880



Internal ID9311000
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 Flag1
Merged StatusS
Merged Variantsesv2656840
Supporting Variants
SamplesNA18501
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5792880
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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