A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8978465



Internal ID13826556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98573823..98573902hg38UCSC Ensembl
InnerchrX:98573819..98573906hg38UCSC Ensembl
OuterchrX:98573740..98573985hg38UCSC Ensembl
chrX:97828821..97828900hg19UCSC Ensembl
InnerchrX:97828817..97828904hg19UCSC Ensembl
OuterchrX:97828738..97828983hg19UCSC Ensembl
chrX:97715477..97715556hg18UCSC Ensembl
InnerchrX:97715560..97715473hg18UCSC Ensembl
OuterchrX:97715394..97715639hg18UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3868
hg1968
hg1868
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3323437
Supporting Variants
SamplesNA18507
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8978465
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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