A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955786



Internal ID16957973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136273277..136275757hg38UCSC Ensembl
Outerchr6:136594415..136596895hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382481
hg192481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002278
SamplesBILGI_BIOE
Known GenesBCLAF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955786
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