A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669209



Internal ID9935314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2447656..2470023hg38UCSC Ensembl
chrX:2365697..2388064hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3822368
hg1922368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6322879
SamplesNA19434
Known GenesDHRSX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669209
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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