A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11317800



Internal ID3280112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3895736..4169659hg38UCSC Ensembl
Innerchr4:3896236..4169159hg38UCSC Ensembl
Outerchr4:3894736..4170659hg38UCSC Ensembl
chr4:3897463..4171386hg19UCSC Ensembl
Innerchr4:3897963..4170886hg19UCSC Ensembl
Outerchr4:3896463..4172386hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38273924
hg19273924
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599439
Supporting Variants
SamplesHG02891
Known GenesFAM86EP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11317800
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