A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5996078



Internal ID8973481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36018902..36019655hg38UCSC Ensembl
chr4:36020524..36021277hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658514
Supporting Variants
SamplesNA19985
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5996078
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