A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6122326



Internal ID8749535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132805403..132807514hg38UCSC Ensembl
chrX:131939431..131941542hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg382112
hg192112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657460
Supporting Variants
SamplesHG00139
Known GenesHS6ST2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6122326
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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