A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5796145



Internal ID9452407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13664776..13668894hg38UCSC Ensembl
chr3:13706276..13710394hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384119
hg194119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664651
Supporting Variants
SamplesNA18871
Known GenesLINC00620
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5796145
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