A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6013806



Internal ID8744613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8817894..8820292hg38UCSC Ensembl
chrX:8785935..8788333hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg382399
hg192399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676276
Supporting Variants
SamplesHG00136
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6013806
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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