A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541026



Internal ID18742102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1455521..1456211hg38UCSC Ensembl
Outerchr7:1455351..1456351hg38UCSC Ensembl
Innerchr7:1495157..1495847hg19UCSC Ensembl
Outerchr7:1494987..1495987hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739773
Samples
Known GenesMICALL2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541026
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