A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8809618



Internal ID13654395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46951697..46971306hg38UCSC Ensembl
InnerchrX:46953277..46969632hg38UCSC Ensembl
OuterchrX:46951582..46971306hg38UCSC Ensembl
chrX:46810487..46830412hg19UCSC Ensembl
InnerchrX:46812477..46828832hg19UCSC Ensembl
OuterchrX:46810377..46830532hg19UCSC Ensembl
chrX:46695431..46715356hg18UCSC Ensembl
InnerchrX:46697421..46713776hg18UCSC Ensembl
OuterchrX:46695321..46715476hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3819610
hg1919926
hg1819926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3336988
Supporting Variants
SamplesNA12878
Known GenesJADE3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8809618
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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