A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673929



Internal ID9940034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5563755..5578517hg38UCSC Ensembl
chrX:5481796..5496558hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3814763
hg1914763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5864226
SamplesNA20515
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673929
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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