A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9857356



Internal ID6482649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12796178..12833339hg38UCSC Ensembl
chr1:12856327..12893193hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3837162
hg1936867
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585243
Supporting Variants
SamplesHG03049
Known GenesPRAMEF1, PRAMEF11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9857356
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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