A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6186583



Internal ID9122589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37991517..37995112hg38UCSC Ensembl
chrX:37850770..37854365hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg383596
hg193596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675672
Supporting Variants
SamplesHG01136
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6186583
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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