A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6451568



Internal ID9786302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94232047..94233008hg38UCSC Ensembl
chrX:93487046..93488007hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670632
Supporting Variants
SamplesNA19777
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6451568
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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