A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5696202



Internal ID8673605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155560528..155573651hg38UCSC Ensembl
chrX:154790189..154803312hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3813124
hg1913124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659146
Supporting Variants
SamplesHG00171
Known GenesTMLHE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5696202
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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