A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665272



Internal ID9931377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28502659..28507903hg38UCSC Ensembl
chrX:28520776..28526020hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg385245
hg195245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6037323, essv6248341
SamplesNA18953, NA19060
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665272
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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