A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620543



Internal ID6660725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68339428..68382871hg38UCSC Ensembl
chr9:70954344..70997787hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3843444
hg1943444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13504902, essv13504901, essv13504903
SamplesNA19384, HG03600, NA18562
Known GenesPGM5, PGM5-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620543
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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