A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676640



Internal ID9942745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62490039..62504417hg38UCSC Ensembl
OuterchrX:62490005..62504452hg38UCSC Ensembl
InnerchrX:61709509..61723887hg19UCSC Ensembl
OuterchrX:61709475..61723922hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3814448
hg1914448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5737101
SamplesHG00113
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676640
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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