A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661042



Internal ID9927147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:133524129..133529204hg38UCSC Ensembl
OuterchrX:133524092..133529254hg38UCSC Ensembl
InnerchrX:132658157..132663232hg19UCSC Ensembl
OuterchrX:132658120..132663282hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg385163
hg195163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6253160
SamplesNA20812
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661042
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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