A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3397621



Internal ID14897898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14711540..14713726hg38UCSC Ensembl
InnerchrX:14712146..14713530hg38UCSC Ensembl
OuterchrX:14711430..14713846hg38UCSC Ensembl
chrX:14729662..14731848hg19UCSC Ensembl
InnerchrX:14730268..14731652hg19UCSC Ensembl
OuterchrX:14729552..14731968hg19UCSC Ensembl
chrX:14639583..14641769hg18UCSC Ensembl
InnerchrX:14641573..14640189hg18UCSC Ensembl
OuterchrX:14639473..14641889hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg382187
hg192187
hg182187
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809604
SamplesNA12878
Known GenesGLRA2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3397621
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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