A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659804



Internal ID9925909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93054534..93104060hg38UCSC Ensembl
OuterchrX:93054497..93104110hg38UCSC Ensembl
InnerchrX:92309533..92359059hg19UCSC Ensembl
OuterchrX:92309496..92359109hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3849614
hg1949614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6184792
SamplesNA19247
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659804
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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