A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9681280



Internal ID14564462
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 StatusS
Merged Variantsesv3398945
Supporting Variants
SamplesNA19141
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9681280
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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