A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4609e59



Internal ID20131358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119900261..119924559hg38UCSC Ensembl
chrX:119034224..119058522hg19UCSC Ensembl
chrX:118918252..118942550hg18UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3824299
hg1924299
hg1824299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3381888, esv3376744
SamplesNA19239, NA19240
Known GenesAKAP14
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4609e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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