A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5826657



Internal ID8792627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8818480..8820841hg38UCSC Ensembl
chrX:8786521..8788882hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg382362
hg192362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674783
Supporting Variants
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5826657
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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