A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6585015



Internal ID9153633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109330374..109332063hg38UCSC Ensembl
chrX:108573603..108575292hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658981
Supporting Variants
SamplesHG01342
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6585015
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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