A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3432532



Internal ID15279488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27813252..27813266hg38UCSC Ensembl
InnerchrX:27813245..27813270hg38UCSC Ensembl
OuterchrX:27813231..27813287hg38UCSC Ensembl
chrX:27831369..27831383hg19UCSC Ensembl
InnerchrX:27831362..27831387hg19UCSC Ensembl
OuterchrX:27831348..27831404hg19UCSC Ensembl
chrX:27741290..27741304hg18UCSC Ensembl
InnerchrX:27741308..27741283hg18UCSC Ensembl
OuterchrX:27741269..27741325hg18UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8677574, essv8677573
SamplesNA19239, NA19240
Known GenesMAGEB10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3432532
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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