A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677573



Internal ID15057483
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 StatusS
Merged Variantsesv3432532
Supporting Variants
SamplesNA19239
Known GenesMAGEB10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677573
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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