A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11653089



Internal ID1654905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150736590..150739044hg38UCSC Ensembl
Innerchr4:150736619..150739016hg38UCSC Ensembl
Outerchr4:150736562..150739073hg38UCSC Ensembl
chr4:151657742..151660196hg19UCSC Ensembl
Innerchr4:151657771..151660168hg19UCSC Ensembl
Outerchr4:151657714..151660225hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382455
hg192455
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602661
Supporting Variants
SamplesHG02657
Known GenesLRBA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11653089
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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