A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7755890



Internal ID14838560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36334545..36334546hg38UCSC Ensembl
InnerchrX:36334473..36334618hg38UCSC Ensembl
OuterchrX:36334472..36334619hg38UCSC Ensembl
chrX:36352660..36352661hg19UCSC Ensembl
InnerchrX:36352588..36352733hg19UCSC Ensembl
OuterchrX:36352587..36352734hg19UCSC Ensembl
chrX:36262581..36262582hg18UCSC Ensembl
InnerchrX:36262654..36262509hg18UCSC Ensembl
OuterchrX:36262508..36262655hg18UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3888
hg1988
hg1888
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3304487
Supporting Variants
SamplesNA19102
Known GenesCXorf30
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7755890
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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