A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5606671



Internal ID8584074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155652443..155663824hg38UCSC Ensembl
chrX:154882104..154893485hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3811382
hg1911382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674660
Supporting Variants
SamplesNA19072
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5606671
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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