A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666911



Internal ID9933016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1451152..1451793hg38UCSC Ensembl
chrX:1570045..1570686hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5976393, essv6467498
SamplesNA18977, NA19776
Known GenesASMTL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666911
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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