A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6312527



Internal ID9444589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111564551..111564965hg38UCSC Ensembl
chrX:110807779..110808193hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669681
Supporting Variants
SamplesNA18858
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6312527
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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