A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434749



Internal ID15281703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26792614..26803612hg38UCSC Ensembl
InnerchrX:26793614..26802612hg38UCSC Ensembl
OuterchrX:26791614..26804612hg38UCSC Ensembl
chrX:26810731..26821729hg19UCSC Ensembl
InnerchrX:26811731..26820729hg19UCSC Ensembl
OuterchrX:26809731..26822729hg19UCSC Ensembl
chrX:26720652..26731650hg18UCSC Ensembl
InnerchrX:26721652..26730650hg18UCSC Ensembl
OuterchrX:26719652..26732650hg18UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3810999
hg1910999
hg1810999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697539
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434749
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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