A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5864226



Internal ID9849261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5563755..5578517hg38UCSC Ensembl
chrX:5481796..5496558hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3814763
hg1914763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673929
Supporting Variants
SamplesNA20515
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5864226
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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