A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602665



Internal ID6642921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150797315..150800750hg38UCSC Ensembl
chr4:151718467..151721902hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383436
hg193436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1034e214
Supporting Variantsessv11653095, essv11653094
SamplesHG02215, HG03919
Known GenesLRBA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602665
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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