A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659928



Internal ID9926033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62586604..62689703hg38UCSC Ensembl
OuterchrX:62586570..62689738hg38UCSC Ensembl
InnerchrX:61806074..61909173hg19UCSC Ensembl
OuterchrX:61806040..61909208hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38103169
hg19103169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5463961
SamplesNA06986
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659928
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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