A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5906288



Internal ID8883691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:129979840..129984346hg38UCSC Ensembl
OuterchrX:129979269..129984916hg38UCSC Ensembl
InnerchrX:129113816..129118322hg19UCSC Ensembl
OuterchrX:129113245..129118892hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg385648
hg195648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676097
Supporting Variants
SamplesHG01097
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5906288
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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