A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661143



Internal ID9927248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1616201..1616843hg38UCSC Ensembl
OuterchrX:1616164..1616893hg38UCSC Ensembl
InnerchrX:1735094..1735736hg19UCSC Ensembl
OuterchrX:1735057..1735786hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6049969, essv6037950, essv6343661, essv6013140, essv6515564, essv5919676, essv5796263, essv5521515, essv5918221, essv5974711
SamplesHG00318, HG00309, HG00182, HG00326, HG00323, HG00176, NA12718, HG00140, NA18559, HG00366
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661143
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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