A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3398945



Internal ID14899222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15608731..15608750hg38UCSC Ensembl
InnerchrX:15608727..15608754hg38UCSC Ensembl
OuterchrX:15608708..15608773hg38UCSC Ensembl
chrX:15626854..15626873hg19UCSC Ensembl
InnerchrX:15626850..15626877hg19UCSC Ensembl
OuterchrX:15626831..15626896hg19UCSC Ensembl
chrX:15536775..15536794hg18UCSC Ensembl
InnerchrX:15536798..15536771hg18UCSC Ensembl
OuterchrX:15536752..15536817hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9681280
SamplesNA19141
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3398945
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer