A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677572



Internal ID15099149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25960305..25960338hg38UCSC Ensembl
InnerchrX:25960310..25960333hg38UCSC Ensembl
OuterchrX:25960277..25960366hg38UCSC Ensembl
chrX:25978422..25978455hg19UCSC Ensembl
InnerchrX:25978427..25978450hg19UCSC Ensembl
OuterchrX:25978394..25978483hg19UCSC Ensembl
chrX:25888343..25888376hg18UCSC Ensembl
InnerchrX:25888371..25888348hg18UCSC Ensembl
OuterchrX:25888315..25888404hg18UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38218
hg19218
hg18218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3402276
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677572
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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