A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6147611



Internal ID9125014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101160034..101164091hg38UCSC Ensembl
chr4:102081191..102085248hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384058
hg194058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677866
Supporting Variants
SamplesHG01375
Known GenesPPP3CA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6147611
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