A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5692887



Internal ID8997883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94145915..94149722hg38UCSC Ensembl
chrX:93400914..93404721hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383808
hg193808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666371
Supporting Variants
SamplesHG00596
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5692887
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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