A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6543678



Internal ID8906715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65801041..65824226hg38UCSC Ensembl
chrX:65020883..65044068hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3823186
hg1923186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663973
Supporting Variants
SamplesHG00369
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6543678
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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