A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664435



Internal ID4708769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32839087..32839570hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6335769, essv6127420, essv6535540, essv6383177, essv6045455, essv6081683
SamplesNA19077, HG00543, NA18599, NA18989, NA18615, HG00531
Known GenesDMD
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664435
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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