A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6044212



Internal ID9627516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89707903..89708226hg38UCSC Ensembl
chr5:89003720..89004043hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657768
Supporting Variants
SamplesNA19347
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6044212
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