A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657205



Internal ID9923310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:82140180..82160183hg38UCSC Ensembl
OuterchrX:82140143..82160233hg38UCSC Ensembl
InnerchrX:81395629..81415632hg19UCSC Ensembl
OuterchrX:81395592..81415682hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3820091
hg1920091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5829575
SamplesNA19712
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657205
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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