A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664390



Internal ID9930495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151919049..151919713hg38UCSC Ensembl
OuterchrX:151919012..151919763hg38UCSC Ensembl
InnerchrX:151087521..151088185hg19UCSC Ensembl
OuterchrX:151087484..151088235hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6036075
SamplesNA18605
Known GenesMAGEA4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664390
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer