A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665745



Internal ID9931850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1609715..1610512hg38UCSC Ensembl
chrX:1728608..1729405hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5496535, essv6471063, essv5677478, essv6070067, essv5409670, essv6338276, essv5646406, essv5524186
SamplesNA19462, NA20126, NA18907, NA19225, NA19467, NA19438, NA19213, NA19129
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665745
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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