A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741372



Internal ID18715618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149033370..149034339hg38UCSC Ensembl
Outerchr7:149033208..149034373hg38UCSC Ensembl
Innerchr7:148730462..148731431hg19UCSC Ensembl
Outerchr7:148730300..148731465hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741372
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