A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669841



Internal ID9935946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:147343794..147345360hg38UCSC Ensembl
OuterchrX:147343757..147345410hg38UCSC Ensembl
InnerchrX:146425312..146426878hg19UCSC Ensembl
OuterchrX:146425275..146426928hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg381654
hg191654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5867273
SamplesNA19376
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669841
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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