A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641047



Internal ID7027821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65719005..66049190hg38UCSC Ensembl
chr17:63715123..64045308hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38330186
hg19330186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15725000
SamplesHG03736
Known GenesCEP112
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer