A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951746



Internal ID17300620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64467122..64492884hg38UCSC Ensembl
Outerchr9:43004001..43029800hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3825763
hg1925800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999435
SamplesBILGI_BIOE
Known GenesFAM95B1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951746
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