A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5468665



Internal ID9909261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103524028..103554198hg38UCSC Ensembl
chrX:102778956..102809126hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3830171
hg1930171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672539
Supporting Variants
SamplesNA20805
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5468665
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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