A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6415836



Internal ID9393239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3444165..3448343hg38UCSC Ensembl
chr4:3445892..3450070hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg384179
hg194179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662185
Supporting Variants
SamplesHG01080
Known GenesHGFAC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6415836
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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