A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5847412



Internal ID9660799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27019777..27020730hg38UCSC Ensembl
chrX:27037894..27038847hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669074
Supporting Variants
SamplesNA19393
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5847412
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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