A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6048836



Internal ID9412731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128008245..128107757hg38UCSC Ensembl
chrX:127142224..127241736hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3899513
hg1999513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666298
Supporting Variants
SamplesNA18615
Known GenesACTRT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6048836
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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