A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6061378



Internal ID9606790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103601765..103603777hg38UCSC Ensembl
chrX:102856693..102858705hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg382013
hg192013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660393
Supporting Variants
SamplesNA19256
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6061378
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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