A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660882



Internal ID9926987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3267820..3269937hg38UCSC Ensembl
chrX:3185861..3187978hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382118
hg192118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6381660
SamplesHG01173
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660882
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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