A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660855



Internal ID9580274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155548461..155552909hg38UCSC Ensembl
chrX:154778122..154782570hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384449
hg194449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5640602, essv5463751, essv5485873, essv6048947, essv5611993, essv5742437, essv5483804, essv6044384, essv5592948, essv6389846
SamplesNA19469, NA18517, NA19449, NA19701, NA19467, NA19900, NA19213, NA19347, NA19225, HG01108
Known GenesTMLHE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660855
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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