A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599862



Internal ID6986907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21301340..21321163hg38UCSC Ensembl
chr4:21302963..21322786hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3819824
hg1919824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv992e214
Supporting Variantsessv11367478
SamplesHG02339
Known GenesKCNIP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599862
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