A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6526113



Internal ID9184830
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 StatusS
Merged Variantsesv2658498
Supporting Variants
SamplesHG01441
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6526113
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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