A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3426907



Internal ID15273864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103525106..103525138hg38UCSC Ensembl
InnerchrX:103525117..103525124hg38UCSC Ensembl
OuterchrX:103525085..103525159hg38UCSC Ensembl
chrX:102780034..102780066hg19UCSC Ensembl
InnerchrX:102780045..102780052hg19UCSC Ensembl
OuterchrX:102780013..102780087hg19UCSC Ensembl
chrX:102666690..102666722hg18UCSC Ensembl
InnerchrX:102666708..102666701hg18UCSC Ensembl
OuterchrX:102666669..102666743hg18UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38813
hg19813
hg18813
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8978573, essv8978576, essv8978577, essv8978571, essv8978574, essv8978575, essv8978572
SamplesNA18942, NA18964, NA18973, NA18570, NA18576, NA18952, NA18577
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3426907
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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