A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6051982



Internal ID9487007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1603683..1604072hg38UCSC Ensembl
chrX:1722576..1722965hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663210
Supporting Variants
SamplesNA18960
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6051982
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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