A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951524



Internal ID16953711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69324985..69326984hg38UCSC Ensembl
Outerchr9:71939901..71941900hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996903
SamplesBILGI_BIOE
Known GenesFAM189A2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951524
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