A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639865



Internal ID6679955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7292786..7322537hg38UCSC Ensembl
chr17:7196105..7225856hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3829752
hg1929752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15604126
SamplesHG02489
Known GenesEIF5A, GPS2, NEURL4, YBX2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639865
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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