A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620515



Internal ID7007386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62842059..62881440hg38UCSC Ensembl
chr9:66497883..66537264hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3839382
hg1939382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13494539, essv13494542, essv13494540, essv13494541
SamplesNA18510, HG02769, NA19984, HG02373
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620515
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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