A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3237607



Internal ID10910588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3691430..3691485hg38UCSC Ensembl
chrX:3609471..3609526hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7507174
SamplesHuRef
Known GenesPRKX
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3237607
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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