A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7837982



Internal ID15138470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25960303..25960304hg38UCSC Ensembl
InnerchrX:25960243..25960364hg38UCSC Ensembl
OuterchrX:25960242..25960365hg38UCSC Ensembl
chrX:25978420..25978421hg19UCSC Ensembl
InnerchrX:25978360..25978481hg19UCSC Ensembl
OuterchrX:25978359..25978482hg19UCSC Ensembl
chrX:25888341..25888342hg18UCSC Ensembl
InnerchrX:25888402..25888281hg18UCSC Ensembl
OuterchrX:25888280..25888403hg18UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38218
hg19218
hg18218
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308983
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7837982
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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