A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660427



Internal ID9579846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19108990..19117738hg38UCSC Ensembl
chrX:19127108..19135856hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg388749
hg198749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5995586
SamplesHG00244
Known GenesGPR64
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660427
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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