A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662510



Internal ID9928615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1638641..1642384hg38UCSC Ensembl
OuterchrX:1638604..1642434hg38UCSC Ensembl
InnerchrX:1757534..1761277hg19UCSC Ensembl
OuterchrX:1757497..1761327hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg383831
hg193831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6392580, essv5491180
SamplesNA19749, HG00638
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662510
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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