A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5976763



Internal ID9167348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90323367..90325381hg38UCSC Ensembl
chrX:89578366..89580380hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg382015
hg192015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678411
Supporting Variants
SamplesHG01366
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5976763
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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