A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5550455



Internal ID9590458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:89764117..89810823hg38UCSC Ensembl
OuterchrX:89763746..89811193hg38UCSC Ensembl
InnerchrX:89019116..89065822hg19UCSC Ensembl
OuterchrX:89018745..89066192hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3847448
hg1947448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667065
Supporting Variants
SamplesNA19204
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5550455
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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