A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950782



Internal ID16952969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:408935..587963hg38UCSC Ensembl
Outerchr7:448901..627600hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38179029
hg19178700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997586
SamplesBILGI_BIOE
Known GenesFLJ44511, PDGFA, PRKAR1B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950782
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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