A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951363



Internal ID16953550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:77186884..77200783hg38UCSC Ensembl
Outerchr7:76816201..76830100hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3813900
hg1913900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998532
SamplesBILGI_BIOE
Known GenesCCDC146, FGL2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951363
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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