A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664331



Internal ID9583750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:51808789..51810266hg38UCSC Ensembl
OuterchrX:51808752..51810316hg38UCSC Ensembl
InnerchrX:51551885..51553362hg19UCSC Ensembl
OuterchrX:51551848..51553412hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6333623
SamplesNA18635
Known GenesMAGED1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664331
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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