A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656624



Internal ID9576043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141915074..141915477hg38UCSC Ensembl
Outerchr3:141915037..141915527hg38UCSC Ensembl
Innerchr3:141633916..141634319hg19UCSC Ensembl
Outerchr3:141633879..141634369hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5886521, essv6538303
SamplesHG00421, NA19720
Known GenesATP1B3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656624
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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