A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5467849



Internal ID9582004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65894119..65894573hg38UCSC Ensembl
chrX:65113961..65114415hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659842
Supporting Variants
SamplesNA19171
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5467849
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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