A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11871995



Internal ID1873811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39072365..39193316hg38UCSC Ensembl
chr5:39072467..39193418hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38120952
hg19120952
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3604777
Supporting Variants
SamplesNA12717
Known GenesFYB, RICTOR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11871995
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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