A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669590



Internal ID9589009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15412486..15412688hg38UCSC Ensembl
chrX:15430608..15430810hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5659894, essv5923906, essv6100817, essv5710389
SamplesNA18557, NA18637, HG00654, NA18571
Known GenesPIR, PIR-FIGF
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669590
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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