A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658498



Internal ID9924603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1640549..1642413hg38UCSC Ensembl
OuterchrX:1640512..1642463hg38UCSC Ensembl
InnerchrX:1759442..1761306hg19UCSC Ensembl
OuterchrX:1759405..1761356hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381952
hg191952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6526113, essv6155083, essv5764234, essv5851975, essv6565327, essv6136235, essv5631211, essv5867172, essv5695913
SamplesHG01441, NA19777, NA12399, NA20796, NA19731, HG01440, NA19682, NA19685, HG00186
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658498
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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