A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669781



Internal ID9935886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38893145..38895750hg38UCSC Ensembl
chrX:38752398..38755003hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg382606
hg192606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6587948, essv6489474
SamplesNA19383, NA19439
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669781
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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