A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6522887



Internal ID9500290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:153641962..153644268hg38UCSC Ensembl
OuterchrX:153641591..153644638hg38UCSC Ensembl
InnerchrX:152907416..152909722hg19UCSC Ensembl
OuterchrX:152907045..152910092hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg383048
hg193048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666278
Supporting Variants
SamplesNA19780
Known GenesDUSP9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6522887
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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