A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613874



Internal ID7000769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80985666..80991710hg38UCSC Ensembl
Innerchr7:80985666..80991710hg38UCSC Ensembl
Outerchr7:80985346..80991868hg38UCSC Ensembl
chr7:80614982..80621026hg19UCSC Ensembl
Innerchr7:80614982..80621026hg19UCSC Ensembl
Outerchr7:80614662..80621184hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg386045
hg196045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12861914, essv12861913, essv12861912, essv12861915
SamplesHG02895, HG03520, NA19440, NA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613874
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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