A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541962



Internal ID18743038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78728550..78728844hg38UCSC Ensembl
Outerchr7:78728511..78728906hg38UCSC Ensembl
Innerchr7:78357866..78358160hg19UCSC Ensembl
Outerchr7:78357827..78358222hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740709
Samples
Known GenesMAGI2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541962
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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